Canonical Allele Identifier: CA1111331316
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs1809947485
gnomAD v3: 8-16992900-T-C
gnomAD v4: 8-16992900-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992900T>C , CM000670.2:g.16992900T>C GRCh38
NC_000008.10:g.16850409T>C , CM000670.1:g.16850409T>C GRCh37
NC_000008.9:g.16894780T>C NCBI36
NG_015978.1:g.14266A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000180166.6:c.*172A>G MANE Select ENSP00000180166.5:n.*172A>G
ENST00000180166.5:c.*172A>G ENSP00000180166.5:n.*172A>G
NM_019851.2:c.*172A>G NP_062825.1:n.*172A>G
NM_019851.3:c.*172A>G MANE Select NP_062825.1:n.*172A>G
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