Canonical Allele Identifier: CA580052654
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs1199490603
gnomAD v2: 8-16850320-G-A
gnomAD v3: 8-16992811-G-A
gnomAD v4: 8-16992811-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992811G>A , CM000670.2:g.16992811G>A GRCh38
NC_000008.10:g.16850320G>A , CM000670.1:g.16850320G>A GRCh37
NC_000008.9:g.16894691G>A NCBI36
NG_015978.1:g.14355C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000180166.6:c.*261C>T MANE Select ENSP00000180166.5:n.*261C>T
ENST00000180166.5:c.*261C>T ENSP00000180166.5:n.*261C>T
NM_019851.3:c.*261C>T MANE Select NP_062825.1:n.*261C>T