Canonical Allele Identifier: CA459633934
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs1181065536
gnomAD v2: 8-16850707-G-A
gnomAD v4: 8-16993198-G-A
MyVariant Identifiers: chr8:g.16850707G>A (hg19) chr8:g.16993198G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993198G>A , CM000670.2:g.16993198G>A GRCh38
NC_000008.10:g.16850707G>A , CM000670.1:g.16850707G>A GRCh37
NC_000008.9:g.16895078G>A NCBI36
NG_015978.1:g.13968C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.510C>T MANE Select ENSP00000180166.5:p.Asn170=
ENST00000180166.5:c.510C>T ENSP00000180166.5:p.Asn170=
ENST00000519941.1:c.214C>T
NM_019851.2:c.510C>T NP_062825.1:p.Asn170=
NM_019851.3:c.510C>T MANE Select NP_062825.1:p.Asn170=
Search 100 bp 5'
Search 100 bp 3'