Canonical Allele Identifier: CA1427629870

Gene:

Linked Data

• dbSNP Id: rs1715477349

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.187931533A>G , CM000665.2:g.187931533A>G	GRCh38
NC_000003.11:g.187649321A>G , CM000665.1:g.187649321A>G	GRCh37
NC_000003.10:g.189132015A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_924814.1:n.1381T>C