Linked Data
ClinVar Variation Id:
413024
dbSNP Id:
rs765750009
ExAC:
17:29677202 T / G
gnomAD v2:
17-29677202-T-G
gnomAD v3:
17-31350184-T-G
gnomAD v4:
17-31350184-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.31350184T>G , CM000679.2:g.31350184T>G | GRCh38 |
| NC_000017.10:g.29677202T>G , CM000679.1:g.29677202T>G | GRCh37 |
| NC_000017.9:g.26701328T>G | NCBI36 |
| NG_009018.1:g.260208T>G , LRG_214:g.260208T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696138.1:c.7305T>G | ENSP00000512431.1:p.Ala2435= | |
| ENST00000684826.1:c.1887T>G | ENSP00000509994.1:p.Ala629= | |
| ENST00000687027.1:c.1479T>G | ENSP00000508715.1:p.Ala493= | |
| ENST00000687863.1:n.3968T>G | ||
| ENST00000689464.1:c.373T>G | ||
| ENST00000691014.1:c.7353T>G | ENSP00000510595.1:p.Ala2451= | |
| ENST00000693617.1:c.1887T>G | ENSP00000510031.1:p.Ala629= | |
| ENST00000358273.9:c.7323T>G MANE Select | ENSP00000351015.4:p.Ala2441= | |
| ENST00000356175.7:c.7260T>G | ENSP00000348498.3:p.Ala2420= | |
| ENST00000358273.8:c.7323T>G | ENSP00000351015.4:p.Ala2441= | |
| ENST00000456735.6:c.6258T>G | ENSP00000389907.2:p.Ala2086= | |
| ENST00000471572.6:c.706T>G | ||
| ENST00000579081.5:c.7459T>G | ENSP00000462408.1:n.7459T>G | |
| ENST00000581790.5:c.466T>G | ||
| NM_000267.3:c.7260T>G , LRG_214t1:c.7260T>G | NP_000258.1:p.Ala2420= | |
| NM_001042492.2:c.7323T>G , LRG_214t2:c.7323T>G | NP_001035957.1:p.Ala2441= | |
| XM_005257983.1:c.7323T>G | XP_005258040.1:p.Ala2441= | |
| XM_005257984.1:c.7260T>G | XP_005258041.1:p.Ala2420= | |
| XM_006721922.1:c.7353T>G | XP_006721985.1:p.Ala2451= | |
| XM_006721923.2:c.7314T>G | XP_006721986.1:p.Ala2438= | |
| XM_006721924.1:c.7353T>G | XP_006721987.1:p.Ala2451= | |
| XM_006721925.1:c.7290T>G | XP_006721988.1:p.Ala2430= | |
| XM_006721926.2:c.7353T>G | XP_006721989.1:p.Ala2451= | |
| XM_006721927.1:c.7353T>G | XP_006721990.1:p.Ala2451= | |
| XM_011524852.1:c.7350T>G | XP_011523154.1:p.Ala2450= | |
| XM_011524853.1:c.7314T>G | XP_011523155.1:p.Ala2438= | |
| XM_011524854.1:c.7314T>G | XP_011523156.1:p.Ala2438= | |
| XM_011524855.1:c.7314T>G | XP_011523157.1:p.Ala2438= | |
| XM_011524856.1:c.7314T>G | XP_011523158.1:p.Ala2438= | |
| XM_011524857.1:c.7353T>G | XP_011523159.1:p.Ala2451= | |
| NM_001042492.3:c.7323T>G MANE Select | NP_001035957.1:p.Ala2441= |