Canonical Allele Identifier: CA4641579
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs767120553
ExAC: 8:16850725 C / T
gnomAD v2: 8-16850725-C-T
gnomAD v4: 8-16993216-C-T
MyVariant Identifiers: chr8:g.16850725C>T (hg19) chr8:g.16993216C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993216C>T , CM000670.2:g.16993216C>T GRCh38
NC_000008.10:g.16850725C>T , CM000670.1:g.16850725C>T GRCh37
NC_000008.9:g.16895096C>T NCBI36
NG_015978.1:g.13950G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.492G>A MANE Select ENSP00000180166.5:p.Arg164=
ENST00000180166.5:c.492G>A ENSP00000180166.5:p.Arg164=
ENST00000519941.1:c.196G>A
NM_019851.2:c.492G>A NP_062825.1:p.Arg164=
NM_019851.3:c.492G>A MANE Select NP_062825.1:p.Arg164=
Search 100 bp 5'
Search 100 bp 3'