Canonical Allele Identifier: CA1057529109
Gene:

Linked Data

dbSNP Id: rs1715477545

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.187931541C>T , CM000665.2:g.187931541C>T GRCh38
NC_000003.11:g.187649329C>T , CM000665.1:g.187649329C>T GRCh37
NC_000003.10:g.189132023C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924814.1:n.1373G>A