Canonical Allele Identifier: CA1841175622
Gene:

Linked Data

dbSNP Id: rs7028097

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551492G>A , CM000671.2:g.25551492G>A GRCh38
NC_000009.11:g.25551490G>A , CM000671.1:g.25551490G>A GRCh37
NC_000009.10:g.25541490G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-920C>T
XR_929525.2:n.674-920C>T