Canonical Allele Identifier: CA2519555322
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v4: 8-16992981-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992981G>C , CM000670.2:g.16992981G>C GRCh38
NC_000008.10:g.16850490G>C , CM000670.1:g.16850490G>C GRCh37
NC_000008.9:g.16894861G>C NCBI36
NG_015978.1:g.14185C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*91C>G MANE Select ENSP00000180166.5:n.*91C>G
ENST00000180166.5:c.*91C>G ENSP00000180166.5:n.*91C>G
ENST00000519941.1:c.431C>G
NM_019851.2:c.*91C>G NP_062825.1:n.*91C>G
NM_019851.3:c.*91C>G MANE Select NP_062825.1:n.*91C>G
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