Canonical Allele Identifier: CA309406868
Gene: FAM83E HGNC NCBI

Linked Data

dbSNP Id: rs558260877
gnomAD v2: 19-49118387-C-T
gnomAD v3: 19-48615130-C-T
gnomAD v4: 19-48615130-C-T
MyVariant Identifiers: chr19:g.49118387C>T (hg19) chr19:g.48615130C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48615130C>T , CM000681.2:g.48615130C>T GRCh38
NC_000019.9:g.49118387C>T , CM000681.1:g.49118387C>T GRCh37
NC_000019.8:g.53810199C>T NCBI36
NG_029867.1:g.840C>T

Transcript Alleles

HGVS Amino-acid change
XM_024451561.1:c.-1577G>A XP_024307329.1:n.-1577G>A
Search 100 bp 5'
Search 100 bp 3'