Canonical Allele Identifier: CA740538605

Gene:

Linked Data

• dbSNP Id: rs1205650100
• MyVariant Identifiers: chr1:g.95029531C>A (hg19) ; chr1:g.94563975C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94563975C>A , CM000663.2:g.94563975C>A	GRCh38
NC_000001.10:g.95029531C>A , CM000663.1:g.95029531C>A	GRCh37
NC_000001.9:g.94802119C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001738161.1:n.461+362C>A