Canonical Allele Identifier: CA740538634

Gene:

Linked Data

• dbSNP Id: rs1176118640
• MyVariant Identifiers: chr1:g.95029605A>T (hg19) ; chr1:g.94564049A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94564049A>T , CM000663.2:g.94564049A>T	GRCh38
NC_000001.10:g.95029605A>T , CM000663.1:g.95029605A>T	GRCh37
NC_000001.9:g.94802193A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001738161.1:n.461+436A>T