Canonical Allele Identifier: CA370394423
Gene: FGF20 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.16850711A>C (hg19) chr8:g.16993202A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993202A>C , CM000670.2:g.16993202A>C GRCh38
NC_000008.10:g.16850711A>C , CM000670.1:g.16850711A>C GRCh37
NC_000008.9:g.16895082A>C NCBI36
NG_015978.1:g.13964T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.506T>G MANE Select ENSP00000180166.5:p.Leu169Arg
ENST00000180166.5:c.506T>G ENSP00000180166.5:p.Leu169Arg
ENST00000519941.1:c.210T>G
NM_019851.2:c.506T>G NP_062825.1:p.Leu169Arg
NM_019851.3:c.506T>G MANE Select NP_062825.1:p.Leu169Arg
Search 100 bp 5'
Search 100 bp 3'