Canonical Allele Identifier: CA32988058

Gene:

Linked Data

• dbSNP Id: rs773327407
• MyVariant Identifiers: chr1:g.172710929A>T (hg19) ; chr1:g.172741789A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.172741789A>T , CM000663.2:g.172741789A>T	GRCh38
NC_000001.10:g.172710929A>T , CM000663.1:g.172710929A>T	GRCh37
NC_000001.9:g.170977552A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_922289.1:n.27-34030A>T