Canonical Allele Identifier: CA2136398888
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50856939T= , CM000676.2:g.50856939T= GRCh38
NC_000014.8:g.51323657T= , CM000676.1:g.51323657T= GRCh37
NC_000014.7:g.50393407T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943848.1:n.282+1159A=
XR_943848.2:n.643+1159A=