Canonical Allele Identifier: CA370394319
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v4: 8-16993151-T-A
MyVariant Identifiers: chr8:g.16850660T>A (hg19) chr8:g.16993151T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993151T>A , CM000670.2:g.16993151T>A GRCh38
NC_000008.10:g.16850660T>A , CM000670.1:g.16850660T>A GRCh37
NC_000008.9:g.16895031T>A NCBI36
NG_015978.1:g.14015A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.557A>T MANE Select ENSP00000180166.5:p.Lys186Ile
ENST00000180166.5:c.557A>T ENSP00000180166.5:p.Lys186Ile
ENST00000519941.1:c.261A>T
NM_019851.2:c.557A>T NP_062825.1:p.Lys186Ile
NM_019851.3:c.557A>T MANE Select NP_062825.1:p.Lys186Ile
Search 100 bp 5'
Search 100 bp 3'