Canonical Allele Identifier: CA1111331289
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v3: 8-16992612-T-C
gnomAD v4: 8-16992612-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992612T>C , CM000670.2:g.16992612T>C GRCh38
NC_000008.10:g.16850121T>C , CM000670.1:g.16850121T>C GRCh37
NC_000008.9:g.16894492T>C NCBI36
NG_015978.1:g.14554A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*460A>G MANE Select ENSP00000180166.5:n.*460A>G
ENST00000180166.5:c.*460A>G ENSP00000180166.5:n.*460A>G
NM_019851.3:c.*460A>G MANE Select NP_062825.1:n.*460A>G
Search 100 bp 5'
Search 100 bp 3'