Canonical Allele Identifier: CA172903779

Gene: FGF20

Linked Data

• ClinVar Variation Id: 1271718
• ClinVar RCV Id: RCV001684292
• dbSNP Id: rs2640901
• gnomAD v2: 8-16850416-A-G
• gnomAD v3: 8-16992907-A-G
• gnomAD v4: 8-16992907-A-G
• MyVariant Identifiers: chr8:g.16850416A>G (hg19) ; chr8:g.16992907A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.16992907A>G , CM000670.2:g.16992907A>G	GRCh38
NC_000008.10:g.16850416A>G , CM000670.1:g.16850416A>G	GRCh37
NC_000008.9:g.16894787A>G	NCBI36
NG_015978.1:g.14259T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000180166.6:c.*165T>C MANE Select	ENSP00000180166.5:n.*165T>C
ENST00000180166.5:c.*165T>C	ENSP00000180166.5:n.*165T>C
NM_019851.2:c.*165T>C	NP_062825.1:n.*165T>C
NM_019851.3:c.*165T>C MANE Select	NP_062825.1:n.*165T>C