Canonical Allele Identifier: CA2339985384
Gene: FAM83E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48615149G= , CM000681.2:g.48615149G= GRCh38
NC_000019.9:g.49118406G= , CM000681.1:g.49118406G= GRCh37
NC_000019.8:g.53810218G= NCBI36
NG_029867.1:g.859G=

Transcript Alleles

HGVS Amino-acid change
XM_024451561.1:c.-1596C= XP_024307329.1:n.-1596C=