Canonical Allele Identifier: CA1841175434
Gene:

Linked Data

dbSNP Id: rs1237623522

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551167A>C , CM000671.2:g.25551167A>C GRCh38
NC_000009.11:g.25551165A>C , CM000671.1:g.25551165A>C GRCh37
NC_000009.10:g.25541165A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929525.1:n.50-595T>G
XR_929525.2:n.674-595T>G