Linked Data
dbSNP Id:
rs147215488
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.44265034C>G , CM000673.2:g.44265034C>G | GRCh38 |
| NC_000011.9:g.44286584C>G , CM000673.1:g.44286584C>G | GRCh37 |
| NC_000011.8:g.44243160C>G | NCBI36 |
| NG_015809.1:g.50133G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000652299.1:c.1056G>C MANE Select | ENSP00000498217.1:p.Val352= | |
| ENST00000329255.3:c.1056G>C | ENSP00000332744.3:p.Val352= | |
| NM_021926.3:c.1056G>C | NP_068745.2:p.Val352= | |
| XM_011520265.1:c.534G>C | XP_011518567.1:p.Val178= | |
| XM_011520266.1:c.534G>C | XP_011518568.1:p.Val178= | |
| NM_021926.4:c.1056G>C MANE Select | NP_068745.2:p.Val352= |