Canonical Allele Identifier: CA2686252139
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v4: 8-16992381-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992381G>T , CM000670.2:g.16992381G>T GRCh38
NC_000008.10:g.16849890G>T , CM000670.1:g.16849890G>T GRCh37
NC_000008.9:g.16894261G>T NCBI36
NG_015978.1:g.14785C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*691C>A MANE Select ENSP00000180166.5:n.*691C>A
ENST00000180166.5:c.*691C>A ENSP00000180166.5:n.*691C>A
NM_019851.3:c.*691C>A MANE Select NP_062825.1:n.*691C>A
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