Canonical Allele Identifier: CA1496030149
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134601490C= , CM000666.2:g.134601490C= GRCh38
NC_000004.11:g.135522645C= , CM000666.1:g.135522645C= GRCh37
NC_000004.10:g.135742095C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939212.1:n.410+14131C=
XR_939214.1:n.392+14131C=
XR_939214.2:n.392+14131C=