Canonical Allele Identifier: CA2716624361
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs2150433363

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992803G>A , CM000670.2:g.16992803G>A GRCh38
NC_000008.10:g.16850312G>A , CM000670.1:g.16850312G>A GRCh37
NC_000008.9:g.16894683G>A NCBI36
NG_015978.1:g.14363C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000180166.6:c.*269C>T MANE Select ENSP00000180166.5:n.*269C>T
ENST00000180166.5:c.*269C>T ENSP00000180166.5:n.*269C>T
NM_019851.3:c.*269C>T MANE Select NP_062825.1:n.*269C>T