Canonical Allele Identifier: CA580052655
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs1255945759
gnomAD v2: 8-16850335-T-C
gnomAD v3: 8-16992826-T-C
gnomAD v4: 8-16992826-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992826T>C , CM000670.2:g.16992826T>C GRCh38
NC_000008.10:g.16850335T>C , CM000670.1:g.16850335T>C GRCh37
NC_000008.9:g.16894706T>C NCBI36
NG_015978.1:g.14340A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000180166.6:c.*246A>G MANE Select ENSP00000180166.5:n.*246A>G
ENST00000180166.5:c.*246A>G ENSP00000180166.5:n.*246A>G
NM_019851.2:c.*246A>G NP_062825.1:n.*246A>G
NM_019851.3:c.*246A>G MANE Select NP_062825.1:n.*246A>G