Canonical Allele Identifier: CA2580595933
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v4: 8-16992890-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992890G>T , CM000670.2:g.16992890G>T GRCh38
NC_000008.10:g.16850399G>T , CM000670.1:g.16850399G>T GRCh37
NC_000008.9:g.16894770G>T NCBI36
NG_015978.1:g.14276C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000180166.6:c.*182C>A MANE Select ENSP00000180166.5:n.*182C>A
ENST00000180166.5:c.*182C>A ENSP00000180166.5:n.*182C>A
NM_019851.2:c.*182C>A NP_062825.1:n.*182C>A
NM_019851.3:c.*182C>A MANE Select NP_062825.1:n.*182C>A
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