Canonical Allele Identifier: CA172903776
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs779979768
gnomAD v2: 8-16850415-A-AG
gnomAD v3: 8-16992906-A-AG
gnomAD v4: 8-16992906-A-AG
MyVariant Identifiers: chr8:g.16850415_16850416insG (hg19) chr8:g.16992906_16992907insG (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992906_16992907insG , CM000670.2:g.16992906_16992907insG GRCh38
NC_000008.10:g.16850415_16850416insG , CM000670.1:g.16850415_16850416insG GRCh37
NC_000008.9:g.16894786_16894787insG NCBI36
NG_015978.1:g.14259_14260insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*165_*166insC MANE Select ENSP00000180166.5:n.*165_*166insC
ENST00000180166.5:c.*165_*166insC ENSP00000180166.5:n.*165_*166insC
NM_019851.2:c.*165_*166insC NP_062825.1:n.*165_*166insC
NM_019851.3:c.*165_*166insC MANE Select NP_062825.1:n.*165_*166insC
Search 100 bp 5'
Search 100 bp 3'