Canonical Allele Identifier: CA2530649801
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134601507T>C , CM000666.2:g.134601507T>C GRCh38
NC_000004.11:g.135522662T>C , CM000666.1:g.135522662T>C GRCh37
NC_000004.10:g.135742112T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939212.1:n.410+14148T>C
XR_939214.1:n.392+14148T>C
XR_939214.2:n.392+14148T>C