Canonical Allele Identifier: CA2339985369
Gene: FAM83E HGNC NCBI

Linked Data

dbSNP Id: rs1974129615
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48615124G>C , CM000681.2:g.48615124G>C GRCh38
NC_000019.9:g.49118381G>C , CM000681.1:g.49118381G>C GRCh37
NC_000019.8:g.53810193G>C NCBI36
NG_029867.1:g.834G>C

Transcript Alleles

HGVS Amino-acid change
XM_024451561.1:c.-1571C>G XP_024307329.1:n.-1571C>G
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