Canonical Allele Identifier: CA129965452

Gene:

Linked Data

• dbSNP Id: rs909567931
• MyVariant Identifiers: chr5:g.159007933C>G (hg19) ; chr5:g.159580925C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159580925C>G , CM000667.2:g.159580925C>G	GRCh38
NC_000005.9:g.159007933C>G , CM000667.1:g.159007933C>G	GRCh37
NC_000005.8:g.158940511C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_941139.1:n.2075+490C>G
XR_941140.1:n.2075+490C>G
XR_941141.1:n.570+490C>G
XR_941139.2:n.2229+490C>G