Canonical Allele Identifier: CA890857331

Gene:

Linked Data

• dbSNP Id: rs1168661425
• MyVariant Identifiers: chr1:g.168618756C>T (hg19) ; chr1:g.168649518C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168649518C>T , CM000663.2:g.168649518C>T	GRCh38
NC_000001.10:g.168618756C>T , CM000663.1:g.168618756C>T	GRCh37
NC_000001.9:g.166885380C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_922259.1:n.201-8243G>A
XR_922259.2:n.332-8243G>A