Canonical Allele Identifier: CA1767395306
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs1809933951
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992390_16992392dup , CM000670.2:g.16992390_16992392dup GRCh38
NC_000008.10:g.16849899_16849901dup , CM000670.1:g.16849899_16849901dup GRCh37
NC_000008.9:g.16894270_16894272dup NCBI36
NG_015978.1:g.14777_14779dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*683_*685dup MANE Select ENSP00000180166.5:n.*683_*685dup
ENST00000180166.5:c.*683_*685dup ENSP00000180166.5:n.*683_*685dup
NM_019851.3:c.*683_*685dup MANE Select NP_062825.1:n.*683_*685dup
Search 100 bp 5'
Search 100 bp 3'