Canonical Allele Identifier:
CA1581765869
Gene:
Linked Data
dbSNP Id:
rs1758562227
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.129387074G>A , CM000667.2:g.129387074G>A | GRCh38 |
| NC_000005.9:g.128722767G>A , CM000667.1:g.128722767G>A | GRCh37 |
| NC_000005.8:g.128750666G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_427770.2:n.163-1374G>A | ||
| XR_948774.1:n.235-5577G>A | ||
| XR_001742463.1:n.4089-1374G>A | ||
| XR_001742464.1:n.2019-5577G>A | ||
| XR_001742465.1:n.401-1374G>A | ||
| XR_427770.3:n.337-1374G>A |