Canonical Allele Identifier: CA2339985379
Gene: FAM83E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48615134C= , CM000681.2:g.48615134C= GRCh38
NC_000019.9:g.49118391C= , CM000681.1:g.49118391C= GRCh37
NC_000019.8:g.53810203C= NCBI36
NG_029867.1:g.844C=

Transcript Alleles

HGVS Amino-acid change
XM_024451561.1:c.-1581G= XP_024307329.1:n.-1581G=