Canonical Allele Identifier: CA172903406
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs1020404581
gnomAD v3: 8-16992577-T-C
gnomAD v4: 8-16992577-T-C
MyVariant Identifiers: chr8:g.16850086T>C (hg19) chr8:g.16992577T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992577T>C , CM000670.2:g.16992577T>C GRCh38
NC_000008.10:g.16850086T>C , CM000670.1:g.16850086T>C GRCh37
NC_000008.9:g.16894457T>C NCBI36
NG_015978.1:g.14589A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*495A>G MANE Select ENSP00000180166.5:n.*495A>G
ENST00000180166.5:c.*495A>G ENSP00000180166.5:n.*495A>G
NM_019851.3:c.*495A>G MANE Select NP_062825.1:n.*495A>G
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