Canonical Allele Identifier: CA521109362

Gene:

Linked Data

• dbSNP Id: rs1315025128
• gnomAD v2: 1-9151141-C-T
• MyVariant Identifiers: chr1:g.9151141C>T (hg19) ; chr1:g.9091082C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.9091082C>T , CM000663.2:g.9091082C>T	GRCh38
NC_000001.10:g.9151141C>T , CM000663.1:g.9151141C>T	GRCh37
NC_000001.9:g.9073728C>T	NCBI36
NG_050918.1:g.7326G>A