Linked Data
dbSNP Id:
rs772723977
ExAC:
5:176519957 G / T
gnomAD v2:
5-176519957-G-T
gnomAD v4:
5-177092956-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.177092956G>T , CM000667.2:g.177092956G>T | GRCh38 |
| NC_000005.9:g.176519957G>T , CM000667.1:g.176519957G>T | GRCh37 |
| NC_000005.8:g.176452563G>T | NCBI36 |
| NG_012067.1:g.11037G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000292408.9:c.1057+172G>T MANE Select | ENSP00000292408.4:n.1057+172G>T | |
| ENST00000292408.8:c.1057+172G>T | ENSP00000292408.4:n.1057+172G>T | |
| ENST00000393637.5:c.1057+172G>T | ENSP00000377254.1:n.1057+172G>T | |
| ENST00000393648.6:c.1057+172G>T | ENSP00000377259.2:n.1057+172G>T | |
| ENST00000502906.5:c.1057+172G>T | ENSP00000424960.1:n.1057+172G>T | |
| ENST00000508139.1:n.361+172G>T | ||
| ENST00000509511.5:n.1229G>T | ||
| NM_001291980.1:c.1057+172G>T | NP_001278909.1:n.1057+172G>T | |
| NM_002011.4:c.1057+172G>T | NP_002002.3:n.1057+172G>T | |
| NM_022963.3:c.1057+172G>T | NP_075252.2:n.1057+172G>T | |
| NM_213647.2:c.1057+172G>T | NP_998812.1:n.1057+172G>T | |
| XM_005265838.2:c.1057+172G>T | XP_005265895.1:n.1057+172G>T | |
| XM_011534464.1:c.1150+172G>T | XP_011532766.1:n.1150+172G>T | |
| XM_011534465.1:c.739+172G>T | XP_011532767.1:n.739+172G>T | |
| XR_941090.1:n.1102+172G>T | ||
| NM_001354984.1:c.1057+172G>T | NP_001341913.1:n.1057+172G>T | |
| NM_213647.3:c.1057+172G>T MANE Select | NP_998812.1:n.1057+172G>T | |
| NM_001291980.2:c.1057+172G>T | NP_001278909.1:n.1057+172G>T | |
| NM_001354984.2:c.1057+172G>T | NP_001341913.1:n.1057+172G>T | |
| NM_002011.5:c.1057+172G>T | NP_002002.3:n.1057+172G>T |