Canonical Allele Identifier: CA2686252258
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v4: 8-16992703-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992703T>C , CM000670.2:g.16992703T>C GRCh38
NC_000008.10:g.16850212T>C , CM000670.1:g.16850212T>C GRCh37
NC_000008.9:g.16894583T>C NCBI36
NG_015978.1:g.14463A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*369A>G MANE Select ENSP00000180166.5:n.*369A>G
ENST00000180166.5:c.*369A>G ENSP00000180166.5:n.*369A>G
NM_019851.3:c.*369A>G MANE Select NP_062825.1:n.*369A>G