Canonical Allele Identifier: CA1111331264
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs1809933681
gnomAD v3: 8-16992382-C-A
gnomAD v4: 8-16992382-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992382C>A , CM000670.2:g.16992382C>A GRCh38
NC_000008.10:g.16849891C>A , CM000670.1:g.16849891C>A GRCh37
NC_000008.9:g.16894262C>A NCBI36
NG_015978.1:g.14784G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*690G>T MANE Select ENSP00000180166.5:n.*690G>T
ENST00000180166.5:c.*690G>T ENSP00000180166.5:n.*690G>T
NM_019851.3:c.*690G>T MANE Select NP_062825.1:n.*690G>T
Search 100 bp 5'
Search 100 bp 3'