Canonical Allele Identifier: CA370394444
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs1161426917
MyVariant Identifiers: chr8:g.16850721A>G (hg19) chr8:g.16993212A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993212A>G , CM000670.2:g.16993212A>G GRCh38
NC_000008.10:g.16850721A>G , CM000670.1:g.16850721A>G GRCh37
NC_000008.9:g.16895092A>G NCBI36
NG_015978.1:g.13954T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.496T>C MANE Select ENSP00000180166.5:p.Phe166Leu
ENST00000180166.5:c.496T>C ENSP00000180166.5:p.Phe166Leu
ENST00000519941.1:c.200T>C
NM_019851.2:c.496T>C NP_062825.1:p.Phe166Leu
NM_019851.3:c.496T>C MANE Select NP_062825.1:p.Phe166Leu
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