Canonical Allele Identifier: CA849279804

Gene: FGF20

Linked Data

• dbSNP Id: rs1322893471
• gnomAD v3: 8-16992501-T-A
• gnomAD v4: 8-16992501-T-A
• MyVariant Identifiers: chr8:g.16850010T>A (hg19) ; chr8:g.16992501T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.16992501T>A , CM000670.2:g.16992501T>A	GRCh38
NC_000008.10:g.16850010T>A , CM000670.1:g.16850010T>A	GRCh37
NC_000008.9:g.16894381T>A	NCBI36
NG_015978.1:g.14665A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000180166.6:c.*571A>T MANE Select	ENSP00000180166.5:n.*571A>T
ENST00000180166.5:c.*571A>T	ENSP00000180166.5:n.*571A>T
NM_019851.3:c.*571A>T MANE Select	NP_062825.1:n.*571A>T