Canonical Allele Identifier: CA2002397752
Gene:

Linked Data

dbSNP Id: rs1864210131

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116072545C>T , CM000673.2:g.116072545C>T GRCh38
NC_000011.9:g.115943263C>T , CM000673.1:g.115943263C>T GRCh37
NC_000011.8:g.115448473C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948055.1:n.192+469G>A
XR_948056.1:n.311-5340G>A
XR_948057.1:n.97+564G>A
XR_001748401.1:n.192+469G>A
XR_948055.2:n.192+469G>A
XR_948056.2:n.314-5340G>A
XR_948057.2:n.97+564G>A