Canonical Allele Identifier: CA2339985386
Gene: FAM83E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48615151A= , CM000681.2:g.48615151A= GRCh38
NC_000019.9:g.49118408A= , CM000681.1:g.49118408A= GRCh37
NC_000019.8:g.53810220A= NCBI36
NG_029867.1:g.861A=

Transcript Alleles

HGVS Amino-acid change
XM_024451561.1:c.-1598T= XP_024307329.1:n.-1598T=