Canonical Allele Identifier: CA942547565
Gene:

Linked Data

dbSNP Id: rs1237258671

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116072508G>T , CM000673.2:g.116072508G>T GRCh38
NC_000011.9:g.115943226G>T , CM000673.1:g.115943226G>T GRCh37
NC_000011.8:g.115448436G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948055.1:n.192+506C>A
XR_948056.1:n.311-5303C>A
XR_948057.1:n.97+601C>A
XR_001748401.1:n.192+506C>A
XR_948055.2:n.192+506C>A
XR_948056.2:n.314-5303C>A
XR_948057.2:n.97+601C>A