Canonical Allele Identifier: CA229980969
Gene:

Linked Data

dbSNP Id: rs1035761278

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116072460T>C , CM000673.2:g.116072460T>C GRCh38
NC_000011.9:g.115943178T>C , CM000673.1:g.115943178T>C GRCh37
NC_000011.8:g.115448388T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948055.1:n.192+554A>G
XR_948056.1:n.311-5255A>G
XR_948057.1:n.97+649A>G
XR_001748401.1:n.192+554A>G
XR_948055.2:n.192+554A>G
XR_948056.2:n.314-5255A>G
XR_948057.2:n.97+649A>G