Linked Data
dbSNP Id:
rs1778866804
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.160076939G>T , CM000668.2:g.160076939G>T | GRCh38 |
| NC_000006.11:g.160497971G>T , CM000668.1:g.160497971G>T | GRCh37 |
| NC_000006.10:g.160417961G>T | NCBI36 |
| NG_011785.3:g.112841G>T | |
| NG_011785.4:g.112841G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356956.6:c.5316+943G>T MANE Select | ENSP00000349437.1:n.5316+943G>T | |
| ENST00000650503.1:n.1926+943G>T | ||
| ENST00000676781.1:c.*3424+943G>T | ENSP00000504419.1:n.*3424+943G>T | |
| ENST00000677704.1:c.*1187+943G>T | ENSP00000503314.1:n.*1187+943G>T | |
| ENST00000356956.5:c.5316+943G>T | ENSP00000349437.1:n.5316+943G>T | |
| NM_000876.2:c.5316+943G>T | NP_000867.2:n.5316+943G>T | |
| NM_000876.3:c.5316+943G>T | NP_000867.2:n.5316+943G>T | |
| NM_000876.4:c.5316+943G>T MANE Select | NP_000867.3:n.5316+943G>T |