Linked Data
ClinVar Variation Id:
508342
dbSNP Id:
rs756124653
ExAC:
15:67457652 C / T
gnomAD v2:
15-67457652-C-T
gnomAD v3:
15-67165314-C-T
gnomAD v4:
15-67165314-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.67165314C>T , CM000677.2:g.67165314C>T | GRCh38 |
| NC_000015.9:g.67457652C>T , CM000677.1:g.67457652C>T | GRCh37 |
| NC_000015.8:g.65244706C>T | NCBI36 |
| NG_011990.1:g.104458C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000558739.2:c.147C>T | ENSP00000453684.2:p.Asp49= | |
| ENST00000559460.6:c.147C>T | ENSP00000453082.2:p.Asp49= | |
| ENST00000560424.2:c.462C>T | ENSP00000455540.2:p.Asp154= | |
| ENST00000327367.9:c.462C>T MANE Select | ENSP00000332973.4:p.Asp154= | |
| ENST00000679624.1:c.147C>T | ENSP00000505445.1:p.Asp49= | |
| ENST00000681239.1:c.147C>T | ENSP00000505641.1:p.Asp49= | |
| ENST00000327367.8:c.462C>T | ENSP00000332973.4:p.Asp154= | |
| ENST00000439724.7:c.330C>T | ENSP00000401133.3:p.Asp110= | |
| ENST00000540846.6:c.147C>T | ENSP00000437757.2:p.Asp49= | |
| ENST00000558739.1:c.147C>T | ENSP00000453684.1:p.Asp49= | |
| ENST00000558894.5:c.147C>T | ENSP00000458060.1:p.Asp49= | |
| ENST00000559460.5:c.147C>T | ENSP00000453082.1:p.Asp49= | |
| ENST00000559937.1:n.312C>T | ||
| ENST00000560175.5:c.147C>T | ENSP00000455095.1:p.Asp49= | |
| NM_001145102.1:c.147C>T | NP_001138574.1:p.Asp49= | |
| NM_001145103.1:c.330C>T | NP_001138575.1:p.Asp110= | |
| NM_005902.3:c.462C>T | NP_005893.1:p.Asp154= | |
| XM_011521559.1:c.400+226C>T | XP_011519861.1:n.400+226C>T | |
| XM_011521560.1:c.315C>T | XP_011519862.1:p.Asp105= | |
| XM_011521559.3:c.400+226C>T | XP_011519861.1:n.400+226C>T | |
| NM_005902.4:c.462C>T MANE Select | NP_005893.1:p.Asp154= | |
| NM_001145102.2:c.147C>T | NP_001138574.1:p.Asp49= | |
| NM_001145103.2:c.330C>T | NP_001138575.1:p.Asp110= |