Canonical Allele Identifier: CA309406859
Gene: FAM83E HGNC NCBI

Linked Data

dbSNP Id: rs920688282
MyVariant Identifiers: chr19:g.49118384G>A (hg19) chr19:g.48615127G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48615127G>A , CM000681.2:g.48615127G>A GRCh38
NC_000019.9:g.49118384G>A , CM000681.1:g.49118384G>A GRCh37
NC_000019.8:g.53810196G>A NCBI36
NG_029867.1:g.837G>A

Transcript Alleles

HGVS Amino-acid change
XM_024451561.1:c.-1574C>T XP_024307329.1:n.-1574C>T
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