Canonical Allele Identifier: CA126566

Gene:

Linked Data

• MyVariant Identifiers: chr1:g.172627498C>C (hg19) ; chr1:g.172658358C>C (hg38)
• PubMed: PMID:15937082

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.172658358C= , CM000663.2:g.172658358C=	GRCh38
NC_000001.10:g.172627498C= , CM000663.1:g.172627498C=	GRCh37
NC_000001.9:g.170894121C=	NCBI36
NG_007269.1:g.4314C= , LRG_58:g.4314C=