Canonical Allele Identifier: CA459633842
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v4: 8-16993123-C-T
COSMIC: COSM5409123
MyVariant Identifiers: chr8:g.16850632C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993123C>T , CM000670.2:g.16993123C>T GRCh38
NC_000008.10:g.16850632C>T , CM000670.1:g.16850632C>T GRCh37
NC_000008.9:g.16895003C>T NCBI36
NG_015978.1:g.14043G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.585G>A MANE Select ENSP00000180166.5:p.Val195=
ENST00000180166.5:c.585G>A ENSP00000180166.5:p.Val195=
ENST00000519941.1:c.289G>A
NM_019851.2:c.585G>A NP_062825.1:p.Val195=
NM_019851.3:c.585G>A MANE Select NP_062825.1:p.Val195=
Search 100 bp 5'
Search 100 bp 3'