Canonical Allele Identifier: CA370394330
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v4: 8-16993155-G-T
MyVariant Identifiers: chr8:g.16850664G>T (hg19) chr8:g.16993155G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993155G>T , CM000670.2:g.16993155G>T GRCh38
NC_000008.10:g.16850664G>T , CM000670.1:g.16850664G>T GRCh37
NC_000008.9:g.16895035G>T NCBI36
NG_015978.1:g.14011C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.553C>A MANE Select ENSP00000180166.5:p.Gln185Lys
ENST00000180166.5:c.553C>A ENSP00000180166.5:p.Gln185Lys
ENST00000519941.1:c.257C>A
NM_019851.2:c.553C>A NP_062825.1:p.Gln185Lys
NM_019851.3:c.553C>A MANE Select NP_062825.1:p.Gln185Lys
Search 100 bp 5'
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