Canonical Allele Identifier: CA2246165591
Gene:

Linked Data

dbSNP Id: rs1981887552

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137274G>T , CM000679.2:g.8137274G>T GRCh38
NC_000017.10:g.8040592G>T , CM000679.1:g.8040592G>T GRCh37
NC_000017.9:g.7981317G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934202.1:n.183-1575G>T
XR_934203.1:n.70-2203G>T
XR_934202.2:n.414-1575G>T