Canonical Allele Identifier: CA185200392
Gene:

Linked Data

dbSNP Id: rs553733109

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122395782T>A , CM000670.2:g.122395782T>A GRCh38
NC_000008.10:g.123408021T>A , CM000670.1:g.123408021T>A GRCh37
NC_000008.9:g.123477202T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928599.1:n.152+3390A>T
XR_928599.3:n.152+3390A>T