Canonical Allele Identifier: CA370394332

Gene: FGF20

Linked Data

• MyVariant Identifiers: chr8:g.16850665A>T (hg19) ; chr8:g.16993156A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.16993156A>T , CM000670.2:g.16993156A>T	GRCh38
NC_000008.10:g.16850665A>T , CM000670.1:g.16850665A>T	GRCh37
NC_000008.9:g.16895036A>T	NCBI36
NG_015978.1:g.14010T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000180166.6:c.552T>A MANE Select	ENSP00000180166.5:p.His184Gln
ENST00000180166.5:c.552T>A	ENSP00000180166.5:p.His184Gln
ENST00000519941.1:c.256T>A
NM_019851.2:c.552T>A	NP_062825.1:p.His184Gln
NM_019851.3:c.552T>A MANE Select	NP_062825.1:p.His184Gln