Canonical Allele Identifier: CA12738948
Gene:

Linked Data

dbSNP Id: rs2954033

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125481504A>G , CM000670.2:g.125481504A>G GRCh38
NC_000008.10:g.126493746A>G , CM000670.1:g.126493746A>G GRCh37
NC_000008.9:g.126562928A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928628.1:n.256+8190A>G