Canonical Allele Identifier: CA942547603
Gene:

Linked Data

dbSNP Id: rs1864210703

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116072571G>T , CM000673.2:g.116072571G>T GRCh38
NC_000011.9:g.115943289G>T , CM000673.1:g.115943289G>T GRCh37
NC_000011.8:g.115448499G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948055.1:n.192+443C>A
XR_948056.1:n.311-5366C>A
XR_948057.1:n.97+538C>A
XR_001748401.1:n.192+443C>A
XR_948055.2:n.192+443C>A
XR_948056.2:n.314-5366C>A
XR_948057.2:n.97+538C>A