Canonical Allele Identifier: CA172903589

Gene: FGF20

Linked Data

• dbSNP Id: rs999003744
• gnomAD v3: 8-16992787-G-A
• gnomAD v4: 8-16992787-G-A
• MyVariant Identifiers: chr8:g.16850296G>A (hg19) ; chr8:g.16992787G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.16992787G>A , CM000670.2:g.16992787G>A	GRCh38
NC_000008.10:g.16850296G>A , CM000670.1:g.16850296G>A	GRCh37
NC_000008.9:g.16894667G>A	NCBI36
NG_015978.1:g.14379C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000180166.6:c.*285C>T MANE Select	ENSP00000180166.5:n.*285C>T
ENST00000180166.5:c.*285C>T	ENSP00000180166.5:n.*285C>T
NM_019851.3:c.*285C>T MANE Select	NP_062825.1:n.*285C>T