Canonical Allele Identifier: CA2339985385
Gene: FAM83E HGNC NCBI

Linked Data

dbSNP Id: rs1974130192

Genomic Alleles

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

Transcript Alleles

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