Canonical Allele Identifier: CA2686252502
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v4: 8-16992987-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992987C>A , CM000670.2:g.16992987C>A GRCh38
NC_000008.10:g.16850496C>A , CM000670.1:g.16850496C>A GRCh37
NC_000008.9:g.16894867C>A NCBI36
NG_015978.1:g.14179G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*85G>T MANE Select ENSP00000180166.5:n.*85G>T
ENST00000180166.5:c.*85G>T ENSP00000180166.5:n.*85G>T
ENST00000519941.1:c.425G>T
NM_019851.2:c.*85G>T NP_062825.1:n.*85G>T
NM_019851.3:c.*85G>T MANE Select NP_062825.1:n.*85G>T