Canonical Allele Identifier: CA849279815

Gene: FGF20

Linked Data

• dbSNP Id: rs1164959091
• gnomAD v3: 8-16992514-A-T
• gnomAD v4: 8-16992514-A-T
• MyVariant Identifiers: chr8:g.16850023A>T (hg19) ; chr8:g.16992514A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.16992514A>T , CM000670.2:g.16992514A>T	GRCh38
NC_000008.10:g.16850023A>T , CM000670.1:g.16850023A>T	GRCh37
NC_000008.9:g.16894394A>T	NCBI36
NG_015978.1:g.14652T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000180166.6:c.*558T>A MANE Select	ENSP00000180166.5:n.*558T>A
ENST00000180166.5:c.*558T>A	ENSP00000180166.5:n.*558T>A
NM_019851.3:c.*558T>A MANE Select	NP_062825.1:n.*558T>A