Canonical Allele Identifier: CA172903222
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs1020350888
gnomAD v3: 8-16992422-T-C
gnomAD v4: 8-16992422-T-C
MyVariant Identifiers: chr8:g.16849931T>C (hg19) chr8:g.16992422T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992422T>C , CM000670.2:g.16992422T>C GRCh38
NC_000008.10:g.16849931T>C , CM000670.1:g.16849931T>C GRCh37
NC_000008.9:g.16894302T>C NCBI36
NG_015978.1:g.14744A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*650A>G MANE Select ENSP00000180166.5:n.*650A>G
ENST00000180166.5:c.*650A>G ENSP00000180166.5:n.*650A>G
NM_019851.3:c.*650A>G MANE Select NP_062825.1:n.*650A>G
Search 100 bp 5'
Search 100 bp 3'