Canonical Allele Identifier: CA580052395
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs1464032347
gnomAD v2: 8-16850124-C-T
gnomAD v3: 8-16992615-C-T
gnomAD v4: 8-16992615-C-T
MyVariant Identifiers: chr8:g.16850124C>T (hg19) chr8:g.16992615C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992615C>T , CM000670.2:g.16992615C>T GRCh38
NC_000008.10:g.16850124C>T , CM000670.1:g.16850124C>T GRCh37
NC_000008.9:g.16894495C>T NCBI36
NG_015978.1:g.14551G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*457G>A MANE Select ENSP00000180166.5:n.*457G>A
ENST00000180166.5:c.*457G>A ENSP00000180166.5:n.*457G>A
NM_019851.3:c.*457G>A MANE Select NP_062825.1:n.*457G>A
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