Canonical Allele Identifier: CA883025792
Gene: FAM83E HGNC NCBI

Linked Data

dbSNP Id: rs1411776391
gnomAD v3: 19-48615123-A-G
gnomAD v4: 19-48615123-A-G
MyVariant Identifiers: chr19:g.49118380A>G (hg19) chr19:g.48615123A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48615123A>G , CM000681.2:g.48615123A>G GRCh38
NC_000019.9:g.49118380A>G , CM000681.1:g.49118380A>G GRCh37
NC_000019.8:g.53810192A>G NCBI36
NG_029867.1:g.833A>G

Transcript Alleles

HGVS Amino-acid change
XM_024451561.1:c.-1570T>C XP_024307329.1:n.-1570T>C
Search 100 bp 5'
Search 100 bp 3'