Canonical Allele Identifier: CA883025800
Gene: FAM83E HGNC NCBI

Linked Data

dbSNP Id: rs1326794210

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48615141G>A , CM000681.2:g.48615141G>A GRCh38
NC_000019.9:g.49118398G>A , CM000681.1:g.49118398G>A GRCh37
NC_000019.8:g.53810210G>A NCBI36
NG_029867.1:g.851G>A

Transcript Alleles

HGVS Amino-acid change
XM_024451561.1:c.-1588C>T XP_024307329.1:n.-1588C>T