Canonical Allele Identifier: CA849280165
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs1330212653
gnomAD v4: 8-16992969-C-G
MyVariant Identifiers: chr8:g.16850478C>G (hg19) chr8:g.16992969C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992969C>G , CM000670.2:g.16992969C>G GRCh38
NC_000008.10:g.16850478C>G , CM000670.1:g.16850478C>G GRCh37
NC_000008.9:g.16894849C>G NCBI36
NG_015978.1:g.14197G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*103G>C MANE Select ENSP00000180166.5:n.*103G>C
ENST00000180166.5:c.*103G>C ENSP00000180166.5:n.*103G>C
NM_019851.2:c.*103G>C NP_062825.1:n.*103G>C
NM_019851.3:c.*103G>C MANE Select NP_062825.1:n.*103G>C
Search 100 bp 5'
Search 100 bp 3'