Canonical Allele Identifier: CA2716787773
Gene:

Linked Data

dbSNP Id: rs2117094241

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20734901T>C , CM000670.2:g.20734901T>C GRCh38
NC_000008.10:g.20592412T>C , CM000670.1:g.20592412T>C GRCh37
NC_000008.9:g.20636692T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949569.3:n.72-55545T>C