Canonical Allele Identifier: CA125569079

Gene:

Linked Data

• dbSNP Id: rs909613099
• MyVariant Identifiers: chr5:g.112996634G>A (hg19) ; chr5:g.113660937G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.113660937G>A , CM000667.2:g.113660937G>A	GRCh38
NC_000005.9:g.112996634G>A , CM000667.1:g.112996634G>A	GRCh37
NC_000005.8:g.113024533G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001742841.1:n.59+27573G>A