Linked Data
dbSNP Id:
rs1377783929
gnomAD v2:
12-121177131-G-C
gnomAD v3:
12-120739328-G-C
gnomAD v4:
12-120739328-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.120739328G>C , CM000674.2:g.120739328G>C | GRCh38 |
| NC_000012.11:g.121177131G>C , CM000674.1:g.121177131G>C | GRCh37 |
| NC_000012.10:g.119661514G>C | NCBI36 |
| NG_007991.1:g.18561G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000242592.9:c.1119G>C MANE Select | ENSP00000242592.4:p.Val373= | |
| ENST00000242592.8:c.1119G>C | ENSP00000242592.4:p.Val373= | |
| ENST00000411593.2:c.1107G>C | ENSP00000401045.2:p.Val369= | |
| NM_000017.3:c.1119G>C | NP_000008.1:p.Val373= | |
| NM_001302554.1:c.1107G>C | NP_001289483.1:p.Val369= | |
| NM_000017.4:c.1119G>C MANE Select | NP_000008.1:p.Val373= | |
| NM_001302554.2:c.1107G>C | NP_001289483.1:p.Val369= |