Canonical Allele Identifier: CA788952613

Gene:

Linked Data

• dbSNP Id: rs1169414502
• MyVariant Identifiers: chr4:g.150901771C>T (hg19) ; chr4:g.149980619C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.149980619C>T , CM000666.2:g.149980619C>T	GRCh38
NC_000004.11:g.150901771C>T , CM000666.1:g.150901771C>T	GRCh37
NC_000004.10:g.151121221C>T	NCBI36