Linked Data
ClinVar Variation Id:
213781
dbSNP Id:
rs768713596
ExAC:
15:67457303 C / T
gnomAD v2:
15-67457303-C-T
gnomAD v4:
15-67164965-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.67164965C>T , CM000677.2:g.67164965C>T | GRCh38 |
| NC_000015.9:g.67457303C>T , CM000677.1:g.67457303C>T | GRCh37 |
| NC_000015.8:g.65244357C>T | NCBI36 |
| NG_011990.1:g.104109C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000558739.2:c.-39C>T | ENSP00000453684.2:n.-39C>T | |
| ENST00000559460.6:c.-39C>T | ENSP00000453082.2:n.-39C>T | |
| ENST00000560424.2:c.277C>T | ENSP00000455540.2:p.Arg93Ter | |
| ENST00000327367.9:c.277C>T MANE Select | ENSP00000332973.4:p.Arg93Ter | |
| ENST00000679624.1:c.-39C>T | ENSP00000505445.1:n.-39C>T | |
| ENST00000681239.1:c.-39C>T | ENSP00000505641.1:n.-39C>T | |
| ENST00000327367.8:c.277C>T | ENSP00000332973.4:p.Arg93Ter | |
| ENST00000439724.7:c.145C>T | ENSP00000401133.3:p.Arg49Ter | |
| ENST00000540846.6:c.-39C>T | ENSP00000437757.2:n.-39C>T | |
| ENST00000558739.1:c.-39C>T | ENSP00000453684.1:n.-39C>T | |
| ENST00000558894.5:c.-39C>T | ENSP00000458060.1:n.-39C>T | |
| ENST00000559092.1:c.222C>T | ENSP00000453788.1:p.Gly74= | |
| ENST00000559460.5:c.-39C>T | ENSP00000453082.1:n.-39C>T | |
| ENST00000559937.1:n.127C>T | ||
| ENST00000560175.5:c.-39C>T | ENSP00000455095.1:n.-39C>T | |
| NM_001145102.1:c.-39C>T | NP_001138574.1:n.-39C>T | |
| NM_001145103.1:c.145C>T | NP_001138575.1:p.Arg49Ter | |
| NM_005902.3:c.277C>T | NP_005893.1:p.Arg93Ter | |
| XM_011521559.1:c.277C>T | XP_011519861.1:p.Arg93Ter | |
| XM_011521560.1:c.130C>T | XP_011519862.1:p.Arg44Ter | |
| XM_011521559.3:c.277C>T | XP_011519861.1:p.Arg93Ter | |
| NM_005902.4:c.277C>T MANE Select | NP_005893.1:p.Arg93Ter | |
| NM_001145102.2:c.-39C>T | NP_001138574.1:n.-39C>T | |
| NM_001145103.2:c.145C>T | NP_001138575.1:p.Arg49Ter |