Linked Data
ClinVar Variation Id:
357415
dbSNP Id:
rs759568939
ExAC:
6:51612709 A / T
gnomAD v2:
6-51612709-A-T
gnomAD v3:
6-51747911-A-T
gnomAD v4:
6-51747911-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.51747911A>T , CM000668.2:g.51747911A>T | GRCh38 |
| NC_000006.11:g.51612709A>T , CM000668.1:g.51612709A>T | GRCh37 |
| NC_000006.10:g.51720668A>T | NCBI36 |
| NG_008753.1:g.344715T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371117.8:c.9705T>A MANE Select | ENSP00000360158.3:p.Asn3235Lys | |
| ENST00000340994.4:c.9705T>A | ENSP00000341097.4:p.Asn3235Lys | |
| ENST00000371117.7:c.9705T>A | ENSP00000360158.3:p.Asn3235Lys | |
| NM_138694.3:c.9705T>A | NP_619639.3:p.Asn3235Lys | |
| NM_170724.2:c.9705T>A | NP_733842.2:p.Asn3235Lys | |
| XM_011514679.1:c.9705T>A | XP_011512981.1:p.Asn3235Lys | |
| XM_011514680.1:c.9705T>A | XP_011512982.1:p.Asn3235Lys | |
| XM_011514681.1:c.9576T>A | XP_011512983.1:p.Asn3192Lys | |
| XM_011514682.1:c.9567T>A | XP_011512984.1:p.Asn3189Lys | |
| XM_011514683.1:c.9063T>A | XP_011512985.1:p.Asn3021Lys | |
| XM_011514684.1:c.8994T>A | XP_011512986.1:p.Asn2998Lys | |
| XM_011514685.1:c.9705T>A | XP_011512987.1:p.Asn3235Lys | |
| XM_011514686.1:c.9705T>A | XP_011512988.1:p.Asn3235Lys | |
| XM_011514687.1:c.9705T>A | XP_011512989.1:p.Asn3235Lys | |
| XM_011514688.1:c.9705T>A | XP_011512990.1:p.Asn3235Lys | |
| XM_011514690.1:c.3780T>A | XP_011512992.1:p.Asn1260Lys | |
| XM_011514691.1:c.3780T>A | XP_011512993.1:p.Asn1260Lys | |
| XM_011514680.3:c.9705T>A | XP_011512982.1:p.Asn3235Lys | |
| XM_011514682.3:c.9567T>A | XP_011512984.1:p.Asn3189Lys | |
| XM_011514683.3:c.9063T>A | XP_011512985.1:p.Asn3021Lys | |
| XM_011514684.3:c.8994T>A | XP_011512986.1:p.Asn2998Lys | |
| XM_011514686.2:c.9705T>A | XP_011512988.1:p.Asn3235Lys | |
| XM_011514688.2:c.9705T>A | XP_011512990.1:p.Asn3235Lys | |
| XM_011514690.3:c.3780T>A | XP_011512992.1:p.Asn1260Lys | |
| XM_011514691.3:c.3780T>A | XP_011512993.1:p.Asn1260Lys | |
| XM_017010944.2:c.9705T>A | XP_016866433.1:p.Asn3235Lys | |
| XM_017010945.2:c.9630T>A | XP_016866434.1:p.Asn3210Lys | |
| XM_017010946.2:c.9510T>A | XP_016866435.1:p.Asn3170Lys | |
| XM_017010947.2:c.9441T>A | XP_016866436.1:p.Asn3147Lys | |
| XM_017010948.2:c.8994T>A | XP_016866437.1:p.Asn2998Lys | |
| XM_017010949.2:c.7845T>A | XP_016866438.1:p.Asn2615Lys | |
| XM_017010950.1:c.9705T>A | XP_016866439.1:p.Asn3235Lys | |
| XR_001743469.1:n.9981T>A | ||
| NM_138694.4:c.9705T>A MANE Select | NP_619639.3:p.Asn3235Lys | |
| NM_170724.3:c.9705T>A | NP_733842.2:p.Asn3235Lys |