Canonical Allele Identifier: CA1767395584
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs1809942760
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992715C>G , CM000670.2:g.16992715C>G GRCh38
NC_000008.10:g.16850224C>G , CM000670.1:g.16850224C>G GRCh37
NC_000008.9:g.16894595C>G NCBI36
NG_015978.1:g.14451G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*357G>C MANE Select ENSP00000180166.5:n.*357G>C
ENST00000180166.5:c.*357G>C ENSP00000180166.5:n.*357G>C
NM_019851.3:c.*357G>C MANE Select NP_062825.1:n.*357G>C
Search 100 bp 5'
Search 100 bp 3'