dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.17298523C>G , CM000669.2:g.17298523C>G | GRCh38 |
| NC_000007.13:g.17338147C>G , CM000669.1:g.17338147C>G | GRCh37 |
| NC_000007.12:g.17304672C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000642825.1:c.20+1899C>G | ENSP00000495987.1:n.20+1899C>G | |
| XR_927069.1:n.14G>C | ||
| XR_927070.1:n.14G>C | ||
| XR_927071.1:n.14G>C | ||
| XR_927072.1:n.15G>C | ||
| XR_927073.1:n.16G>C | ||
| XR_927073.2:n.16G>C |