Canonical Allele Identifier: CA370394465
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v4: 8-16993223-C-T
MyVariant Identifiers: chr8:g.16850732C>T (hg19) chr8:g.16993223C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993223C>T , CM000670.2:g.16993223C>T GRCh38
NC_000008.10:g.16850732C>T , CM000670.1:g.16850732C>T GRCh37
NC_000008.9:g.16895103C>T NCBI36
NG_015978.1:g.13943G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.485G>A MANE Select ENSP00000180166.5:p.Gly162Asp
ENST00000180166.5:c.485G>A ENSP00000180166.5:p.Gly162Asp
ENST00000519941.1:c.189G>A
NM_019851.2:c.485G>A NP_062825.1:p.Gly162Asp
NM_019851.3:c.485G>A MANE Select NP_062825.1:p.Gly162Asp
Search 100 bp 5'
Search 100 bp 3'