Canonical Allele Identifier: CA862568086
Gene:

Linked Data

dbSNP Id: rs1372862473

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551288T>C , CM000671.2:g.25551288T>C GRCh38
NC_000009.11:g.25551286T>C , CM000671.1:g.25551286T>C GRCh37
NC_000009.10:g.25541286T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929525.1:n.50-716A>G
XR_929525.2:n.674-716A>G