Canonical Allele Identifier: CA849280157
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs1256091326
gnomAD v3: 8-16992929-C-T
gnomAD v4: 8-16992929-C-T
MyVariant Identifiers: chr8:g.16850438C>T (hg19) chr8:g.16992929C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992929C>T , CM000670.2:g.16992929C>T GRCh38
NC_000008.10:g.16850438C>T , CM000670.1:g.16850438C>T GRCh37
NC_000008.9:g.16894809C>T NCBI36
NG_015978.1:g.14237G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*143G>A MANE Select ENSP00000180166.5:n.*143G>A
ENST00000180166.5:c.*143G>A ENSP00000180166.5:n.*143G>A
NM_019851.2:c.*143G>A NP_062825.1:n.*143G>A
NM_019851.3:c.*143G>A MANE Select NP_062825.1:n.*143G>A
Search 100 bp 5'
Search 100 bp 3'