Canonical Allele Identifier: CA2686252391
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v4: 8-16992892-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992892T>C , CM000670.2:g.16992892T>C GRCh38
NC_000008.10:g.16850401T>C , CM000670.1:g.16850401T>C GRCh37
NC_000008.9:g.16894772T>C NCBI36
NG_015978.1:g.14274A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000180166.6:c.*180A>G MANE Select ENSP00000180166.5:n.*180A>G
ENST00000180166.5:c.*180A>G ENSP00000180166.5:n.*180A>G
NM_019851.2:c.*180A>G NP_062825.1:n.*180A>G
NM_019851.3:c.*180A>G MANE Select NP_062825.1:n.*180A>G