Canonical Allele Identifier: CA580052398
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs1203971295
gnomAD v2: 8-16850127-A-C
gnomAD v3: 8-16992618-A-C
gnomAD v4: 8-16992618-A-C
MyVariant Identifiers: chr8:g.16850127A>C (hg19) chr8:g.16992618A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992618A>C , CM000670.2:g.16992618A>C GRCh38
NC_000008.10:g.16850127A>C , CM000670.1:g.16850127A>C GRCh37
NC_000008.9:g.16894498A>C NCBI36
NG_015978.1:g.14548T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*454T>G MANE Select ENSP00000180166.5:n.*454T>G
ENST00000180166.5:c.*454T>G ENSP00000180166.5:n.*454T>G
NM_019851.3:c.*454T>G MANE Select NP_062825.1:n.*454T>G
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