Canonical Allele Identifier: CA1674885989
Gene:

Linked Data

dbSNP Id: rs1778859682

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812740G>A , CM000668.2:g.155812740G>A GRCh38
NC_000006.11:g.156133874G>A , CM000668.1:g.156133874G>A GRCh37
NC_000006.10:g.156175566G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+19321G>A
XR_943146.1:n.645-701C>T
XR_001744423.1:n.699-701C>T
XR_001744424.1:n.79+19321G>A