Canonical Allele Identifier: CA1496030176
Gene:

Linked Data

dbSNP Id: rs1578687533

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134601570T>C , CM000666.2:g.134601570T>C GRCh38
NC_000004.11:g.135522725T>C , CM000666.1:g.135522725T>C GRCh37
NC_000004.10:g.135742175T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939212.1:n.410+14211T>C
XR_939214.1:n.392+14211T>C
XR_939214.2:n.392+14211T>C