Canonical Allele Identifier: CA849279952

Gene: FGF20

Linked Data

• dbSNP Id: rs1354541180
• MyVariant Identifiers: chr8:g.16850200C>G (hg19) ; chr8:g.16992691C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.16992691C>G , CM000670.2:g.16992691C>G	GRCh38
NC_000008.10:g.16850200C>G , CM000670.1:g.16850200C>G	GRCh37
NC_000008.9:g.16894571C>G	NCBI36
NG_015978.1:g.14475G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000180166.6:c.*381G>C MANE Select	ENSP00000180166.5:n.*381G>C
ENST00000180166.5:c.*381G>C	ENSP00000180166.5:n.*381G>C
NM_019851.3:c.*381G>C MANE Select	NP_062825.1:n.*381G>C