Canonical Allele Identifier:
CA1557963401
Gene:
Linked Data
dbSNP Id:
rs1753646713
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.79549929G>A , CM000667.2:g.79549929G>A | GRCh38 |
| NC_000005.9:g.78845752G>A , CM000667.1:g.78845752G>A | GRCh37 |
| NC_000005.8:g.78881508G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_948497.1:n.72+2285G>A | ||
| XR_948498.1:n.159+2092G>A | ||
| XR_948499.1:n.67+1627G>A | ||
| XR_948497.2:n.72+2285G>A | ||
| XR_948498.2:n.159+2092G>A | ||
| XR_948499.2:n.225+1627G>A |