Canonical Allele Identifier: CA370394390

Gene: FGF20

Linked Data

• MyVariant Identifiers: chr8:g.16850696G>C (hg19) ; chr8:g.16993187G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.16993187G>C , CM000670.2:g.16993187G>C	GRCh38
NC_000008.10:g.16850696G>C , CM000670.1:g.16850696G>C	GRCh37
NC_000008.9:g.16895067G>C	NCBI36
NG_015978.1:g.13979C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000180166.6:c.521C>G MANE Select	ENSP00000180166.5:p.Thr174Ser
ENST00000180166.5:c.521C>G	ENSP00000180166.5:p.Thr174Ser
ENST00000519941.1:c.225C>G
NM_019851.2:c.521C>G	NP_062825.1:p.Thr174Ser
NM_019851.3:c.521C>G MANE Select	NP_062825.1:p.Thr174Ser