Canonical Allele Identifier: CA172903423

Gene: FGF20

Linked Data

• dbSNP Id: rs750613452
• gnomAD v2: 8-16850112-G-GT
• gnomAD v3: 8-16992603-G-GT
• gnomAD v4: 8-16992603-G-GT
• MyVariant Identifiers: chr8:g.16850113_16850114insT (hg19) ; chr8:g.16850112_16850113insT (hg19) ; chr8:g.16992604_16992605insT (hg38) ; chr8:g.16992603_16992604insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.16992614dup , CM000670.2:g.16992614dup	GRCh38
NC_000008.10:g.16850123dup , CM000670.1:g.16850123dup	GRCh37
NC_000008.9:g.16894494dup	NCBI36
NG_015978.1:g.14562dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000180166.6:c.*468dup MANE Select	ENSP00000180166.5:n.*468dup
ENST00000180166.5:c.*468dup	ENSP00000180166.5:n.*468dup
NM_019851.3:c.*468dup MANE Select	NP_062825.1:n.*468dup