Canonical Allele Identifier: CA890857302

Gene:

Linked Data

• dbSNP Id: rs1310024050
• MyVariant Identifiers: chr1:g.168618713G>T (hg19) ; chr1:g.168649475G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168649475G>T , CM000663.2:g.168649475G>T	GRCh38
NC_000001.10:g.168618713G>T , CM000663.1:g.168618713G>T	GRCh37
NC_000001.9:g.166885337G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_922259.1:n.201-8200C>A
XR_922259.2:n.332-8200C>A