Canonical Allele Identifier: CA787553450
Gene:

Linked Data

dbSNP Id: rs1027180154

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134601547T>C , CM000666.2:g.134601547T>C GRCh38
NC_000004.11:g.135522702T>C , CM000666.1:g.135522702T>C GRCh37
NC_000004.10:g.135742152T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939212.1:n.410+14188T>C
XR_939214.1:n.392+14188T>C
XR_939214.2:n.392+14188T>C