Linked Data
dbSNP Id:
rs2011077
gnomAD v2:
5-176521456-C-T
gnomAD v3:
5-177094455-C-T
gnomAD v4:
5-177094455-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.177094455C>T , CM000667.2:g.177094455C>T | GRCh38 |
| NC_000005.9:g.176521456C>T , CM000667.1:g.176521456C>T | GRCh37 |
| NC_000005.8:g.176454062C>T | NCBI36 |
| NG_012067.1:g.12536C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000292408.9:c.1519+680C>T MANE Select | ENSP00000292408.4:n.1519+680C>T | |
| ENST00000292408.8:c.1519+680C>T | ENSP00000292408.4:n.1519+680C>T | |
| ENST00000393637.5:c.1399+680C>T | ENSP00000377254.1:n.1399+680C>T | |
| ENST00000393648.6:c.1315+680C>T | ENSP00000377259.2:n.1315+680C>T | |
| ENST00000502906.5:c.1519+680C>T | ENSP00000424960.1:n.1519+680C>T | |
| ENST00000511076.1:c.413+680C>T | ||
| NM_001291980.1:c.1315+680C>T | NP_001278909.1:n.1315+680C>T | |
| NM_002011.4:c.1519+680C>T | NP_002002.3:n.1519+680C>T | |
| NM_022963.3:c.1399+680C>T | NP_075252.2:n.1399+680C>T | |
| NM_213647.2:c.1519+680C>T | NP_998812.1:n.1519+680C>T | |
| XM_005265838.2:c.1519+680C>T | XP_005265895.1:n.1519+680C>T | |
| XM_011534464.1:c.1612+680C>T | XP_011532766.1:n.1612+680C>T | |
| XM_011534465.1:c.1201+680C>T | XP_011532767.1:n.1201+680C>T | |
| XR_941090.1:n.1514+680C>T | ||
| NM_001354984.1:c.1519+680C>T | NP_001341913.1:n.1519+680C>T | |
| NM_213647.3:c.1519+680C>T MANE Select | NP_998812.1:n.1519+680C>T | |
| NM_001291980.2:c.1315+680C>T | NP_001278909.1:n.1315+680C>T | |
| NM_001354984.2:c.1519+680C>T | NP_001341913.1:n.1519+680C>T | |
| NM_002011.5:c.1519+680C>T | NP_002002.3:n.1519+680C>T |