Canonical Allele Identifier: CA31701857

Gene:

Linked Data

• dbSNP Id: rs866637807
• MyVariant Identifiers: chr1:g.168618730T>C (hg19) ; chr1:g.168649492T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168649492T>C , CM000663.2:g.168649492T>C	GRCh38
NC_000001.10:g.168618730T>C , CM000663.1:g.168618730T>C	GRCh37
NC_000001.9:g.166885354T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_922259.1:n.201-8217A>G
XR_922259.2:n.332-8217A>G