Linked Data
ClinVar Variation Id:
799484
ClinVar RCV Id:
RCV000983086
dbSNP Id:
rs763463216
ExAC:
6:51524643 T / C
gnomAD v2:
6-51524643-T-C
gnomAD v4:
6-51659845-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.51659845T>C , CM000668.2:g.51659845T>C | GRCh38 |
| NC_000006.11:g.51524643T>C , CM000668.1:g.51524643T>C | GRCh37 |
| NC_000006.10:g.51632602T>C | NCBI36 |
| NG_008753.1:g.432781A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371117.8:c.10281A>G MANE Select | ENSP00000360158.3:p.Leu3427= | |
| ENST00000371117.7:c.10281A>G | ENSP00000360158.3:p.Leu3427= | |
| NM_138694.3:c.10281A>G | NP_619639.3:p.Leu3427= | |
| XM_011514679.1:c.10281A>G | XP_011512981.1:p.Leu3427= | |
| XM_011514680.1:c.10281A>G | XP_011512982.1:p.Leu3427= | |
| XM_011514681.1:c.10152A>G | XP_011512983.1:p.Leu3384= | |
| XM_011514682.1:c.10143A>G | XP_011512984.1:p.Leu3381= | |
| XM_011514683.1:c.9639A>G | XP_011512985.1:p.Leu3213= | |
| XM_011514684.1:c.9570A>G | XP_011512986.1:p.Leu3190= | |
| XM_011514687.1:c.10157-10625A>G | XP_011512989.1:n.10157-10625A>G | |
| XM_011514690.1:c.4356A>G | XP_011512992.1:p.Leu1452= | |
| XM_011514691.1:c.4356A>G | XP_011512993.1:p.Leu1452= | |
| XR_926870.1:n.535+7472T>C | ||
| XR_926871.1:n.403+7472T>C | ||
| XR_926872.1:n.535+7472T>C | ||
| XM_011514680.3:c.10281A>G | XP_011512982.1:p.Leu3427= | |
| XM_011514682.3:c.10143A>G | XP_011512984.1:p.Leu3381= | |
| XM_011514683.3:c.9639A>G | XP_011512985.1:p.Leu3213= | |
| XM_011514684.3:c.9570A>G | XP_011512986.1:p.Leu3190= | |
| XM_011514690.3:c.4356A>G | XP_011512992.1:p.Leu1452= | |
| XM_011514691.3:c.4356A>G | XP_011512993.1:p.Leu1452= | |
| XM_017010944.2:c.10281A>G | XP_016866433.1:p.Leu3427= | |
| XM_017010945.2:c.10206A>G | XP_016866434.1:p.Leu3402= | |
| XM_017010946.2:c.10086A>G | XP_016866435.1:p.Leu3362= | |
| XM_017010947.2:c.10017A>G | XP_016866436.1:p.Leu3339= | |
| XM_017010948.2:c.9570A>G | XP_016866437.1:p.Leu3190= | |
| XM_017010949.2:c.8421A>G | XP_016866438.1:p.Leu2807= | |
| XR_001743469.1:n.10557A>G | ||
| XR_001744157.1:n.3145+7472T>C | ||
| XR_926870.2:n.3145+7472T>C | ||
| XR_926871.2:n.3013+7472T>C | ||
| XR_926872.2:n.3145+7472T>C | ||
| NM_138694.4:c.10281A>G MANE Select | NP_619639.3:p.Leu3427= |