Canonical Allele Identifier: CA1427629978

Gene:

Linked Data

• dbSNP Id: rs1715479191

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.187931636A>G , CM000665.2:g.187931636A>G	GRCh38
NC_000003.11:g.187649424A>G , CM000665.1:g.187649424A>G	GRCh37
NC_000003.10:g.189132118A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_924814.1:n.1278T>C