Canonical Allele Identifier: CA31701818

Gene:

Linked Data

• dbSNP Id: rs909750723
• MyVariant Identifiers: chr1:g.168618678C>T (hg19) ; chr1:g.168649440C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168649440C>T , CM000663.2:g.168649440C>T	GRCh38
NC_000001.10:g.168618678C>T , CM000663.1:g.168618678C>T	GRCh37
NC_000001.9:g.166885302C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_922259.1:n.201-8165G>A
XR_922259.2:n.332-8165G>A