Canonical Allele Identifier: CA459634030
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs1809957955
gnomAD v4: 8-16993234-A-G
MyVariant Identifiers: chr8:g.16850743A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993234A>G , CM000670.2:g.16993234A>G GRCh38
NC_000008.10:g.16850743A>G , CM000670.1:g.16850743A>G GRCh37
NC_000008.9:g.16895114A>G NCBI36
NG_015978.1:g.13932T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.474T>C MANE Select ENSP00000180166.5:p.His158=
ENST00000180166.5:c.474T>C ENSP00000180166.5:p.His158=
ENST00000519941.1:c.178T>C
NM_019851.2:c.474T>C NP_062825.1:p.His158=
NM_019851.3:c.474T>C MANE Select NP_062825.1:p.His158=
Search 100 bp 5'
Search 100 bp 3'