Canonical Allele Identifier: CA185200391
Gene:

Linked Data

dbSNP Id: rs374719282

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122395780A>G , CM000670.2:g.122395780A>G GRCh38
NC_000008.10:g.123408019A>G , CM000670.1:g.123408019A>G GRCh37
NC_000008.9:g.123477200A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928599.1:n.152+3392T>C
XR_928599.3:n.152+3392T>C