Canonical Allele Identifier: CA4641562
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs767173525
ExAC: 8:16850668 C / A
gnomAD v2: 8-16850668-C-A
gnomAD v4: 8-16993159-C-A
MyVariant Identifiers: chr8:g.16850668C>A (hg19) chr8:g.16993159C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993159C>A , CM000670.2:g.16993159C>A GRCh38
NC_000008.10:g.16850668C>A , CM000670.1:g.16850668C>A GRCh37
NC_000008.9:g.16895039C>A NCBI36
NG_015978.1:g.14007G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.549G>T MANE Select ENSP00000180166.5:p.Arg183Ser
ENST00000180166.5:c.549G>T ENSP00000180166.5:p.Arg183Ser
ENST00000519941.1:c.253G>T
NM_019851.2:c.549G>T NP_062825.1:p.Arg183Ser
NM_019851.3:c.549G>T MANE Select NP_062825.1:p.Arg183Ser
Search 100 bp 5'
Search 100 bp 3'