Canonical Allele Identifier: CA1767395856
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs1809949108
gnomAD v4: 8-16992953-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992953C>T , CM000670.2:g.16992953C>T GRCh38
NC_000008.10:g.16850462C>T , CM000670.1:g.16850462C>T GRCh37
NC_000008.9:g.16894833C>T NCBI36
NG_015978.1:g.14213G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*119G>A MANE Select ENSP00000180166.5:n.*119G>A
ENST00000180166.5:c.*119G>A ENSP00000180166.5:n.*119G>A
NM_019851.2:c.*119G>A NP_062825.1:n.*119G>A
NM_019851.3:c.*119G>A MANE Select NP_062825.1:n.*119G>A
Search 100 bp 5'
Search 100 bp 3'