Canonical Allele Identifier: CA185200404
Gene:

Linked Data

dbSNP Id: rs377008863

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122395863G>A , CM000670.2:g.122395863G>A GRCh38
NC_000008.10:g.123408102G>A , CM000670.1:g.123408102G>A GRCh37
NC_000008.9:g.123477283G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928599.1:n.152+3309C>T
XR_928599.3:n.152+3309C>T