Canonical Allele Identifier: CA287548593
Gene:

Linked Data

dbSNP Id: rs994760017

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137596G>T , CM000679.2:g.8137596G>T GRCh38
NC_000017.10:g.8040914G>T , CM000679.1:g.8040914G>T GRCh37
NC_000017.9:g.7981639G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934202.1:n.183-1253G>T
XR_934203.1:n.70-1881G>T
XR_934202.2:n.414-1253G>T