Linked Data
dbSNP Id:
rs764471876
ExAC:
6:51523921 T / A
gnomAD v2:
6-51523921-T-A
gnomAD v4:
6-51659123-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.51659123T>A , CM000668.2:g.51659123T>A | GRCh38 |
| NC_000006.11:g.51523921T>A , CM000668.1:g.51523921T>A | GRCh37 |
| NC_000006.10:g.51631880T>A | NCBI36 |
| NG_008753.1:g.433503A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371117.8:c.11003A>T MANE Select | ENSP00000360158.3:p.Asp3668Val | |
| ENST00000371117.7:c.11003A>T | ENSP00000360158.3:p.Asp3668Val | |
| NM_138694.3:c.11003A>T | NP_619639.3:p.Asp3668Val | |
| XM_011514679.1:c.11003A>T | XP_011512981.1:p.Asp3668Val | |
| XM_011514680.1:c.11003A>T | XP_011512982.1:p.Asp3668Val | |
| XM_011514681.1:c.10874A>T | XP_011512983.1:p.Asp3625Val | |
| XM_011514682.1:c.10865A>T | XP_011512984.1:p.Asp3622Val | |
| XM_011514683.1:c.10361A>T | XP_011512985.1:p.Asp3454Val | |
| XM_011514684.1:c.10292A>T | XP_011512986.1:p.Asp3431Val | |
| XM_011514687.1:c.10157-9903A>T | XP_011512989.1:n.10157-9903A>T | |
| XM_011514690.1:c.5078A>T | XP_011512992.1:p.Asp1693Val | |
| XM_011514691.1:c.5078A>T | XP_011512993.1:p.Asp1693Val | |
| XR_926870.1:n.535+6750T>A | ||
| XR_926871.1:n.403+6750T>A | ||
| XR_926872.1:n.535+6750T>A | ||
| XM_011514680.3:c.11003A>T | XP_011512982.1:p.Asp3668Val | |
| XM_011514682.3:c.10865A>T | XP_011512984.1:p.Asp3622Val | |
| XM_011514683.3:c.10361A>T | XP_011512985.1:p.Asp3454Val | |
| XM_011514684.3:c.10292A>T | XP_011512986.1:p.Asp3431Val | |
| XM_011514690.3:c.5078A>T | XP_011512992.1:p.Asp1693Val | |
| XM_011514691.3:c.5078A>T | XP_011512993.1:p.Asp1693Val | |
| XM_017010944.2:c.11003A>T | XP_016866433.1:p.Asp3668Val | |
| XM_017010945.2:c.10928A>T | XP_016866434.1:p.Asp3643Val | |
| XM_017010946.2:c.10808A>T | XP_016866435.1:p.Asp3603Val | |
| XM_017010947.2:c.10739A>T | XP_016866436.1:p.Asp3580Val | |
| XM_017010948.2:c.10292A>T | XP_016866437.1:p.Asp3431Val | |
| XM_017010949.2:c.9143A>T | XP_016866438.1:p.Asp3048Val | |
| XR_001743469.1:n.11279A>T | ||
| XR_001744157.1:n.3145+6750T>A | ||
| XR_926870.2:n.3145+6750T>A | ||
| XR_926871.2:n.3013+6750T>A | ||
| XR_926872.2:n.3145+6750T>A | ||
| NM_138694.4:c.11003A>T MANE Select | NP_619639.3:p.Asp3668Val |