Canonical Allele Identifier: CA2593751020
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs2150433346
gnomAD v3: 8-16992756-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992756G>T , CM000670.2:g.16992756G>T GRCh38
NC_000008.10:g.16850265G>T , CM000670.1:g.16850265G>T GRCh37
NC_000008.9:g.16894636G>T NCBI36
NG_015978.1:g.14410C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*316C>A MANE Select ENSP00000180166.5:n.*316C>A
ENST00000180166.5:c.*316C>A ENSP00000180166.5:n.*316C>A
NM_019851.3:c.*316C>A MANE Select NP_062825.1:n.*316C>A
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