Canonical Allele Identifier: CA1096189871
Gene:

Linked Data

dbSNP Id: rs1778928171

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155817524G>A , CM000668.2:g.155817524G>A GRCh38
NC_000006.11:g.156138658G>A , CM000668.1:g.156138658G>A GRCh37
NC_000006.10:g.156180350G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943142.1:n.79+24105G>A
XR_943146.1:n.552-2854C>T
XR_001744423.1:n.606-2854C>T
XR_001744424.1:n.79+24105G>A