Canonical Allele Identifier: CA172903328

Gene: FGF20

Linked Data

• dbSNP Id: rs1001460232
• gnomAD v3: 8-16992525-A-C
• gnomAD v4: 8-16992525-A-C
• MyVariant Identifiers: chr8:g.16850034A>C (hg19) ; chr8:g.16992525A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.16992525A>C , CM000670.2:g.16992525A>C	GRCh38
NC_000008.10:g.16850034A>C , CM000670.1:g.16850034A>C	GRCh37
NC_000008.9:g.16894405A>C	NCBI36
NG_015978.1:g.14641T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000180166.6:c.*547T>G MANE Select	ENSP00000180166.5:n.*547T>G
ENST00000180166.5:c.*547T>G	ENSP00000180166.5:n.*547T>G
NM_019851.3:c.*547T>G MANE Select	NP_062825.1:n.*547T>G