Linked Data
dbSNP Id:
rs770088313
ExAC:
11:113803103 C / T
gnomAD v2:
11-113803103-C-T
gnomAD v3:
11-113932381-C-T
gnomAD v4:
11-113932381-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.113932381C>T , CM000673.2:g.113932381C>T | GRCh38 |
| NC_000011.9:g.113803103C>T , CM000673.1:g.113803103C>T | GRCh37 |
| NC_000011.8:g.113308313C>T | NCBI36 |
| NG_011483.1:g.32515C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260191.8:c.461C>T MANE Select | ENSP00000260191.2:p.Ala154Val | |
| ENST00000260191.7:c.461C>T | ENSP00000260191.2:p.Ala154Val | |
| ENST00000260191.6:c.461C>T | ENSP00000260191.2:p.Ala154Val | |
| ENST00000537778.5:c.428C>T | ENSP00000443118.1:p.Ala143Val | |
| ENST00000543092.1:c.247C>T | ||
| NM_006028.4:c.461C>T | NP_006019.1:p.Ala154Val | |
| XM_011543063.1:c.428C>T | XP_011541365.1:p.Ala143Val | |
| XM_011543064.1:c.260C>T | XP_011541366.1:p.Ala87Val | |
| XM_011543065.1:c.254C>T | XP_011541367.1:p.Ala85Val | |
| XM_011543066.1:c.428C>T | XP_011541368.1:p.Ala143Val | |
| NM_001363563.1:c.428C>T | NP_001350492.1:p.Ala143Val | |
| XM_017018552.2:c.254C>T | XP_016874041.1:p.Ala85Val | |
| XM_024448767.1:c.167C>T | XP_024304535.1:p.Ala56Val | |
| XR_001748034.2:n.712C>T | ||
| NM_001363563.2:c.428C>T | NP_001350492.1:p.Ala143Val | |
| NM_006028.5:c.461C>T MANE Select | NP_006019.1:p.Ala154Val |