Linked Data
dbSNP Id:
rs781907541
gnomAD v2:
11-111706978-C-G
gnomAD v3:
11-111836255-C-G
gnomAD v4:
11-111836255-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.111836255C>G , CM000673.2:g.111836255C>G | GRCh38 |
| NC_000011.9:g.111706978C>G , CM000673.1:g.111706978C>G | GRCh37 |
| NC_000011.8:g.111212188C>G | NCBI36 |
| NG_009210.1:g.40327G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000616540.5:c.1512G>C MANE Select | ENSP00000482437.1:p.Gln504His | |
| ENST00000398006.6:c.978G>C | ENSP00000381090.2:p.Gln326His | |
| ENST00000526272.5:n.76G>C | ||
| ENST00000530851.6:n.537+17125G>C | ||
| ENST00000531154.5:c.999G>C | ENSP00000435517.1:p.Gln333His | |
| ENST00000532425.6:c.245G>C | ||
| ENST00000614444.4:c.1491G>C | ENSP00000484200.1:p.Gln497His | |
| ENST00000616540.4:c.1512G>C | ENSP00000482437.1:p.Gln504His | |
| ENST00000619129.4:c.*1043G>C | ENSP00000480661.1:n.*1043G>C | |
| ENST00000622211.4:c.2190G>C | ENSP00000482396.1:p.Gln730His | |
| NM_001077690.1:c.1491G>C | NP_001071158.1:p.Gln497His | |
| NM_001077691.1:c.999G>C | NP_001071159.1:p.Gln333His | |
| NM_001077692.1:c.978G>C | NP_001071160.1:p.Gln326His | |
| NM_024740.2:c.1512G>C MANE Select | NP_079016.2:p.Gln504His | |
| XM_005277723.3:c.1512G>C | XP_005277780.1:p.Gln504His | |
| XM_005277724.3:c.1491G>C | XP_005277781.1:p.Gln497His | |
| XM_006718913.2:c.1512G>C | XP_006718976.1:p.Gln504His | |
| XM_011542990.1:c.1512G>C | XP_011541292.1:p.Gln504His | |
| XM_011542991.1:c.1491G>C | XP_011541293.1:p.Gln497His | |
| XM_011542992.1:c.1512G>C | XP_011541294.1:p.Gln504His | |
| XM_011542993.1:c.999G>C | XP_011541295.1:p.Gln333His | |
| XM_011542994.1:c.999G>C | XP_011541296.1:p.Gln333His | |
| XM_011542995.1:c.999G>C | XP_011541297.1:p.Gln333His | |
| XM_011542996.1:c.999G>C | XP_011541298.1:p.Gln333His | |
| XM_011542997.1:c.924G>C | XP_011541299.1:p.Gln308His | |
| XR_947863.1:n.1611G>C | ||
| XR_947864.1:n.1435G>C | ||
| XR_947865.1:n.1435G>C | ||
| NM_001352409.1:c.978G>C | NP_001339338.1:p.Gln326His | |
| NM_001352410.1:c.978G>C | NP_001339339.1:p.Gln326His | |
| NM_001352411.1:c.978G>C | NP_001339340.1:p.Gln326His | |
| NM_001352412.1:c.978G>C | NP_001339341.1:p.Gln326His | |
| NM_001352413.1:c.999G>C | NP_001339342.1:p.Gln333His | |
| NM_001352414.1:c.999G>C | NP_001339343.1:p.Gln333His | |
| NM_001352415.1:c.978G>C | NP_001339344.1:p.Gln326His | |
| NM_001352416.1:c.978G>C | NP_001339345.1:p.Gln326His | |
| NM_001352417.1:c.1491G>C | NP_001339346.1:p.Gln497His | |
| NM_001352418.1:c.1368G>C | NP_001339347.1:p.Gln456His | |
| NM_001352419.1:c.999G>C | NP_001339348.1:p.Gln333His | |
| NM_001352420.1:c.978G>C | NP_001339349.1:p.Gln326His | |
| NM_001352421.1:c.978G>C | NP_001339350.1:p.Gln326His | |
| NM_001352422.1:c.903G>C | NP_001339351.1:p.Gln301His | |
| NM_001352423.1:c.855G>C | NP_001339352.1:p.Gln285His | |
| NR_147984.1:n.1888G>C | ||
| XM_005277723.5:c.1512G>C | XP_005277780.1:p.Gln504His | |
| XM_006718913.3:c.1512G>C | XP_006718976.1:p.Gln504His | |
| XM_011542992.2:c.1512G>C | XP_011541294.1:p.Gln504His | |
| XM_017018313.2:c.1491G>C | XP_016873802.1:p.Gln497His | |
| XM_017018314.2:c.1389G>C | XP_016873803.1:p.Gln463His | |
| XM_024448695.1:c.1491G>C | XP_024304463.1:p.Gln497His | |
| XR_001747967.2:n.1600G>C | ||
| XR_001747968.2:n.1579G>C | ||
| XR_001747969.2:n.1477G>C | ||
| XR_001747970.2:n.1579G>C | ||
| XR_001747971.1:n.1908G>C | ||
| XR_001747972.1:n.1912G>C | ||
| XR_001747973.1:n.1615G>C | ||
| XR_001747974.1:n.1728G>C | ||
| XR_001747975.1:n.1887G>C | ||
| XR_001747976.1:n.1891G>C | ||
| XR_001747977.1:n.1064G>C | ||
| XR_001747979.1:n.1867G>C | ||
| XR_001747980.1:n.1563G>C | ||
| XR_947863.3:n.1600G>C | ||
| XR_947864.2:n.1424G>C | ||
| XR_947865.2:n.1424G>C | ||
| NM_001077691.2:c.999G>C | NP_001071159.1:p.Gln333His | |
| NM_001077692.2:c.978G>C | NP_001071160.1:p.Gln326His | |
| NM_001352411.2:c.978G>C | NP_001339340.1:p.Gln326His | |
| NM_001352412.2:c.978G>C | NP_001339341.1:p.Gln326His | |
| NM_001352414.2:c.999G>C | NP_001339343.1:p.Gln333His | |
| NM_001352420.2:c.978G>C | NP_001339349.1:p.Gln326His | |
| NM_001352421.2:c.978G>C | NP_001339350.1:p.Gln326His | |
| NM_001352422.2:c.903G>C | NP_001339351.1:p.Gln301His | |
| NM_001352423.2:c.855G>C | NP_001339352.1:p.Gln285His | |
| NR_147984.2:n.1908G>C |