Canonical Allele Identifier: CA2034130509
Gene:

Linked Data

dbSNP Id: rs11610206

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47245743T>A , CM000674.2:g.47245743T>A GRCh38
NC_000012.11:g.47639526T>A , CM000674.1:g.47639526T>A GRCh37
NC_000012.10:g.45925793T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944896.1:n.909+3808A>T
XR_944896.2:n.911+3808A>T