Canonical Allele Identifier: CA580052352
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs1361289940
gnomAD v2: 8-16849923-C-T
gnomAD v3: 8-16992414-C-T
gnomAD v4: 8-16992414-C-T
MyVariant Identifiers: chr8:g.16849923C>T (hg19) chr8:g.16992414C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992414C>T , CM000670.2:g.16992414C>T GRCh38
NC_000008.10:g.16849923C>T , CM000670.1:g.16849923C>T GRCh37
NC_000008.9:g.16894294C>T NCBI36
NG_015978.1:g.14752G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*658G>A MANE Select ENSP00000180166.5:n.*658G>A
ENST00000180166.5:c.*658G>A ENSP00000180166.5:n.*658G>A
NM_019851.3:c.*658G>A MANE Select NP_062825.1:n.*658G>A
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