Canonical Allele Identifier: CA459633896
Gene: FGF20 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.16850680G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993171G>T , CM000670.2:g.16993171G>T GRCh38
NC_000008.10:g.16850680G>T , CM000670.1:g.16850680G>T GRCh37
NC_000008.9:g.16895051G>T NCBI36
NG_015978.1:g.13995C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.537C>A MANE Select ENSP00000180166.5:p.Ala179=
ENST00000180166.5:c.537C>A ENSP00000180166.5:p.Ala179=
ENST00000519941.1:c.241C>A
NM_019851.2:c.537C>A NP_062825.1:p.Ala179=
NM_019851.3:c.537C>A MANE Select NP_062825.1:p.Ala179=
Search 100 bp 5'
Search 100 bp 3'