Canonical Allele Identifier: CA370394431

Gene: FGF20

Linked Data

• MyVariant Identifiers: chr8:g.16850715C>G (hg19) ; chr8:g.16993206C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.16993206C>G , CM000670.2:g.16993206C>G	GRCh38
NC_000008.10:g.16850715C>G , CM000670.1:g.16850715C>G	GRCh37
NC_000008.9:g.16895086C>G	NCBI36
NG_015978.1:g.13960G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000180166.6:c.502G>C MANE Select	ENSP00000180166.5:p.Ala168Pro
ENST00000180166.5:c.502G>C	ENSP00000180166.5:p.Ala168Pro
ENST00000519941.1:c.206G>C
NM_019851.2:c.502G>C	NP_062825.1:p.Ala168Pro
NM_019851.3:c.502G>C MANE Select	NP_062825.1:p.Ala168Pro