Canonical Allele Identifier: CA1427630026

Gene:

Linked Data

• dbSNP Id: rs1715480835

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.187931701C>T , CM000665.2:g.187931701C>T	GRCh38
NC_000003.11:g.187649489C>T , CM000665.1:g.187649489C>T	GRCh37
NC_000003.10:g.189132183C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_924814.1:n.1213G>A