Canonical Allele Identifier: CA370394402
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs762222483
gnomAD v2: 8-16850702-T-C
gnomAD v4: 8-16993193-T-C
MyVariant Identifiers: chr8:g.16850702T>C (hg19) chr8:g.16993193T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993193T>C , CM000670.2:g.16993193T>C GRCh38
NC_000008.10:g.16850702T>C , CM000670.1:g.16850702T>C GRCh37
NC_000008.9:g.16895073T>C NCBI36
NG_015978.1:g.13973A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.515A>G MANE Select ENSP00000180166.5:p.Asp172Gly
ENST00000180166.5:c.515A>G ENSP00000180166.5:p.Asp172Gly
ENST00000519941.1:c.219A>G
NM_019851.2:c.515A>G NP_062825.1:p.Asp172Gly
NM_019851.3:c.515A>G MANE Select NP_062825.1:p.Asp172Gly
Search 100 bp 5'
Search 100 bp 3'