Canonical Allele Identifier: CA2536264194
Gene: FGF20 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992404G>T , CM000670.2:g.16992404G>T GRCh38
NC_000008.10:g.16849913G>T , CM000670.1:g.16849913G>T GRCh37
NC_000008.9:g.16894284G>T NCBI36
NG_015978.1:g.14762C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*668C>A MANE Select ENSP00000180166.5:n.*668C>A
ENST00000180166.5:c.*668C>A ENSP00000180166.5:n.*668C>A
NM_019851.3:c.*668C>A MANE Select NP_062825.1:n.*668C>A
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