Canonical Allele Identifier: CA580052651

Gene: FGF20

Linked Data

• dbSNP Id: rs1264400384
• gnomAD v2: 8-16850295-G-T
• gnomAD v3: 8-16992786-G-T
• gnomAD v4: 8-16992786-G-T
• MyVariant Identifiers: chr8:g.16850295G>T (hg19) ; chr8:g.16992786G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.16992786G>T , CM000670.2:g.16992786G>T	GRCh38
NC_000008.10:g.16850295G>T , CM000670.1:g.16850295G>T	GRCh37
NC_000008.9:g.16894666G>T	NCBI36
NG_015978.1:g.14380C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000180166.6:c.*286C>A MANE Select	ENSP00000180166.5:n.*286C>A
ENST00000180166.5:c.*286C>A	ENSP00000180166.5:n.*286C>A
NM_019851.3:c.*286C>A MANE Select	NP_062825.1:n.*286C>A