Canonical Allele Identifier: CA172903845
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs112602726
gnomAD v3: 8-16992952-T-A
gnomAD v4: 8-16992952-T-A
MyVariant Identifiers: chr8:g.16850461T>A (hg19) chr8:g.16992952T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992952T>A , CM000670.2:g.16992952T>A GRCh38
NC_000008.10:g.16850461T>A , CM000670.1:g.16850461T>A GRCh37
NC_000008.9:g.16894832T>A NCBI36
NG_015978.1:g.14214A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*120A>T MANE Select ENSP00000180166.5:n.*120A>T
ENST00000180166.5:c.*120A>T ENSP00000180166.5:n.*120A>T
NM_019851.2:c.*120A>T NP_062825.1:n.*120A>T
NM_019851.3:c.*120A>T MANE Select NP_062825.1:n.*120A>T
Search 100 bp 5'
Search 100 bp 3'