Canonical Allele Identifier: CA2704846811
Gene:

Linked Data

dbSNP Id: rs2108529018

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.187931543T>C , CM000665.2:g.187931543T>C GRCh38
NC_000003.11:g.187649331T>C , CM000665.1:g.187649331T>C GRCh37
NC_000003.10:g.189132025T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924814.1:n.1371A>G