Canonical Allele Identifier: CA1496030119
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134601441C= , CM000666.2:g.134601441C= GRCh38
NC_000004.11:g.135522596C= , CM000666.1:g.135522596C= GRCh37
NC_000004.10:g.135742046C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939212.1:n.410+14082C=
XR_939214.1:n.392+14082C=
XR_939214.2:n.392+14082C=