Linked Data
ClinVar Variation Id:
2163041
ClinVar RCV Id:
RCV003070553
dbSNP Id:
rs782783433
gnomAD v2:
11-111708313-A-G
gnomAD v3:
11-111837590-A-G
gnomAD v4:
11-111837590-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.111837590A>G , CM000673.2:g.111837590A>G | GRCh38 |
| NC_000011.9:g.111708313A>G , CM000673.1:g.111708313A>G | GRCh37 |
| NC_000011.8:g.111213523A>G | NCBI36 |
| NG_009210.1:g.38992T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000616540.5:c.1350T>C MANE Select | ENSP00000482437.1:p.Tyr450= | |
| ENST00000398006.6:c.816T>C | ENSP00000381090.2:p.Tyr272= | |
| ENST00000527294.5:n.647T>C | ||
| ENST00000530851.6:n.537+15790T>C | ||
| ENST00000531154.5:c.837T>C | ENSP00000435517.1:p.Tyr279= | |
| ENST00000532425.6:c.83T>C | ||
| ENST00000613181.4:c.*751T>C | ENSP00000479335.1:n.*751T>C | |
| ENST00000614444.4:c.1329T>C | ENSP00000484200.1:p.Tyr443= | |
| ENST00000616540.4:c.1350T>C | ENSP00000482437.1:p.Tyr450= | |
| ENST00000619129.4:c.*881T>C | ENSP00000480661.1:n.*881T>C | |
| ENST00000622211.4:c.2028T>C | ENSP00000482396.1:p.Tyr676= | |
| NM_001077690.1:c.1329T>C | NP_001071158.1:p.Tyr443= | |
| NM_001077691.1:c.837T>C | NP_001071159.1:p.Tyr279= | |
| NM_001077692.1:c.816T>C | NP_001071160.1:p.Tyr272= | |
| NM_024740.2:c.1350T>C MANE Select | NP_079016.2:p.Tyr450= | |
| XM_005277723.3:c.1350T>C | XP_005277780.1:p.Tyr450= | |
| XM_005277724.3:c.1329T>C | XP_005277781.1:p.Tyr443= | |
| XM_006718913.2:c.1350T>C | XP_006718976.1:p.Tyr450= | |
| XM_011542990.1:c.1350T>C | XP_011541292.1:p.Tyr450= | |
| XM_011542991.1:c.1329T>C | XP_011541293.1:p.Tyr443= | |
| XM_011542992.1:c.1350T>C | XP_011541294.1:p.Tyr450= | |
| XM_011542993.1:c.837T>C | XP_011541295.1:p.Tyr279= | |
| XM_011542994.1:c.837T>C | XP_011541296.1:p.Tyr279= | |
| XM_011542995.1:c.837T>C | XP_011541297.1:p.Tyr279= | |
| XM_011542996.1:c.837T>C | XP_011541298.1:p.Tyr279= | |
| XM_011542997.1:c.762T>C | XP_011541299.1:p.Tyr254= | |
| XR_947863.1:n.1449T>C | ||
| XR_947864.1:n.1273T>C | ||
| XR_947865.1:n.1273T>C | ||
| NM_001352409.1:c.816T>C | NP_001339338.1:p.Tyr272= | |
| NM_001352410.1:c.816T>C | NP_001339339.1:p.Tyr272= | |
| NM_001352411.1:c.816T>C | NP_001339340.1:p.Tyr272= | |
| NM_001352412.1:c.816T>C | NP_001339341.1:p.Tyr272= | |
| NM_001352413.1:c.837T>C | NP_001339342.1:p.Tyr279= | |
| NM_001352414.1:c.837T>C | NP_001339343.1:p.Tyr279= | |
| NM_001352415.1:c.816T>C | NP_001339344.1:p.Tyr272= | |
| NM_001352416.1:c.816T>C | NP_001339345.1:p.Tyr272= | |
| NM_001352417.1:c.1329T>C | NP_001339346.1:p.Tyr443= | |
| NM_001352418.1:c.1206T>C | NP_001339347.1:p.Tyr402= | |
| NM_001352419.1:c.837T>C | NP_001339348.1:p.Tyr279= | |
| NM_001352420.1:c.816T>C | NP_001339349.1:p.Tyr272= | |
| NM_001352421.1:c.816T>C | NP_001339350.1:p.Tyr272= | |
| NM_001352422.1:c.741T>C | NP_001339351.1:p.Tyr247= | |
| NM_001352423.1:c.693T>C | NP_001339352.1:p.Tyr231= | |
| NR_147984.1:n.1726T>C | ||
| XM_005277723.5:c.1350T>C | XP_005277780.1:p.Tyr450= | |
| XM_006718913.3:c.1350T>C | XP_006718976.1:p.Tyr450= | |
| XM_011542992.2:c.1350T>C | XP_011541294.1:p.Tyr450= | |
| XM_017018313.2:c.1329T>C | XP_016873802.1:p.Tyr443= | |
| XM_017018314.2:c.1227T>C | XP_016873803.1:p.Tyr409= | |
| XM_024448695.1:c.1329T>C | XP_024304463.1:p.Tyr443= | |
| XR_001747967.2:n.1438T>C | ||
| XR_001747968.2:n.1417T>C | ||
| XR_001747969.2:n.1315T>C | ||
| XR_001747970.2:n.1417T>C | ||
| XR_001747971.1:n.1746T>C | ||
| XR_001747972.1:n.1750T>C | ||
| XR_001747973.1:n.1453T>C | ||
| XR_001747974.1:n.1566T>C | ||
| XR_001747975.1:n.1725T>C | ||
| XR_001747976.1:n.1729T>C | ||
| XR_001747977.1:n.902T>C | ||
| XR_001747979.1:n.1705T>C | ||
| XR_001747980.1:n.1401T>C | ||
| XR_947863.3:n.1438T>C | ||
| XR_947864.2:n.1262T>C | ||
| XR_947865.2:n.1262T>C | ||
| NM_001077691.2:c.837T>C | NP_001071159.1:p.Tyr279= | |
| NM_001077692.2:c.816T>C | NP_001071160.1:p.Tyr272= | |
| NM_001352411.2:c.816T>C | NP_001339340.1:p.Tyr272= | |
| NM_001352412.2:c.816T>C | NP_001339341.1:p.Tyr272= | |
| NM_001352414.2:c.837T>C | NP_001339343.1:p.Tyr279= | |
| NM_001352420.2:c.816T>C | NP_001339349.1:p.Tyr272= | |
| NM_001352421.2:c.816T>C | NP_001339350.1:p.Tyr272= | |
| NM_001352422.2:c.741T>C | NP_001339351.1:p.Tyr247= | |
| NM_001352423.2:c.693T>C | NP_001339352.1:p.Tyr231= | |
| NR_147984.2:n.1746T>C |