Canonical Allele Identifier: CA32988068

Gene:

Linked Data

• dbSNP Id: rs906951520
• gnomAD v2: 1-172711003-C-T
• gnomAD v3: 1-172741863-C-T
• gnomAD v4: 1-172741863-C-T
• MyVariant Identifiers: chr1:g.172711003C>T (hg19) ; chr1:g.172741863C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.172741863C>T , CM000663.2:g.172741863C>T	GRCh38
NC_000001.10:g.172711003C>T , CM000663.1:g.172711003C>T	GRCh37
NC_000001.9:g.170977626C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_922289.1:n.27-33956C>T