Canonical Allele Identifier: CA2727598592
Gene:

Linked Data

dbSNP Id: rs2136272153

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.131529665A>G , CM000674.2:g.131529665A>G GRCh38
NC_000012.11:g.132014210A>G , CM000674.1:g.132014210A>G GRCh37
NC_000012.10:g.130580163A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945564.1:n.1076+110T>C
XR_001749407.2:n.1067+110T>C