Canonical Allele Identifier: CA31701718

Gene:

Linked Data

• dbSNP Id: rs1008893612
• MyVariant Identifiers: chr1:g.168618446G>A (hg19) ; chr1:g.168649208G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168649208G>A , CM000663.2:g.168649208G>A	GRCh38
NC_000001.10:g.168618446G>A , CM000663.1:g.168618446G>A	GRCh37
NC_000001.9:g.166885070G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_922259.1:n.201-7933C>T
XR_922259.2:n.332-7933C>T