Canonical Allele Identifier: CA287548598
Gene:

Linked Data

dbSNP Id: rs950349604

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137610G>T , CM000679.2:g.8137610G>T GRCh38
NC_000017.10:g.8040928G>T , CM000679.1:g.8040928G>T GRCh37
NC_000017.9:g.7981653G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934202.1:n.183-1239G>T
XR_934203.1:n.70-1867G>T
XR_934202.2:n.414-1239G>T