Canonical Allele Identifier: CA2699825017
Gene:

Linked Data

dbSNP Id: rs2104020673

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.81645867G>T , CM000664.2:g.81645867G>T GRCh38
NC_000002.11:g.81872991G>T , CM000664.1:g.81872991G>T GRCh37
NC_000002.10:g.81726502G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940294.1:n.563+66258G>T
XR_940295.1:n.485+97120G>T
XR_001739571.1:n.485+97120G>T