Linked Data
dbSNP Id:
rs1772000627
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.41751136C>T , CM000668.2:g.41751136C>T | GRCh38 |
| NC_000006.11:g.41718874C>T , CM000668.1:g.41718874C>T | GRCh37 |
| NC_000006.10:g.41826852C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000415707.1:c.71+2762G>A | ENSP00000399429.1:n.71+2762G>A |