Canonical Allele Identifier: CA1767395852
Gene: FGF20 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992946C= , CM000670.2:g.16992946C= GRCh38
NC_000008.10:g.16850455C= , CM000670.1:g.16850455C= GRCh37
NC_000008.9:g.16894826C= NCBI36
NG_015978.1:g.14220G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*126G= MANE Select ENSP00000180166.5:n.*126G=
ENST00000180166.5:c.*126G= ENSP00000180166.5:n.*126G=
NM_019851.2:c.*126G= NP_062825.1:n.*126G=
NM_019851.3:c.*126G= MANE Select NP_062825.1:n.*126G=
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