Canonical Allele Identifier: CA229981107
Gene:

Linked Data

dbSNP Id: rs915341441

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116072523A>C , CM000673.2:g.116072523A>C GRCh38
NC_000011.9:g.115943241A>C , CM000673.1:g.115943241A>C GRCh37
NC_000011.8:g.115448451A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948055.1:n.192+491T>G
XR_948056.1:n.311-5318T>G
XR_948057.1:n.97+586T>G
XR_001748401.1:n.192+491T>G
XR_948055.2:n.192+491T>G
XR_948056.2:n.314-5318T>G
XR_948057.2:n.97+586T>G