Canonical Allele Identifier: CA185200387
Gene:

Linked Data

dbSNP Id: rs370682752

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122395761G>A , CM000670.2:g.122395761G>A GRCh38
NC_000008.10:g.123408000G>A , CM000670.1:g.123408000G>A GRCh37
NC_000008.9:g.123477181G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928599.1:n.152+3411C>T
XR_928599.3:n.152+3411C>T