Canonical Allele Identifier: CA2136398938
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50857046T= , CM000676.2:g.50857046T= GRCh38
NC_000014.8:g.51323764T= , CM000676.1:g.51323764T= GRCh37
NC_000014.7:g.50393514T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943848.1:n.282+1052A=
XR_943848.2:n.643+1052A=