Canonical Allele Identifier: CA4641582
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs143400495
ExAC: 8:16850733 C / T
gnomAD v2: 8-16850733-C-T
gnomAD v4: 8-16993224-C-T
MyVariant Identifiers: chr8:g.16850733C>T (hg19) chr8:g.16993224C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993224C>T , CM000670.2:g.16993224C>T GRCh38
NC_000008.10:g.16850733C>T , CM000670.1:g.16850733C>T GRCh37
NC_000008.9:g.16895104C>T NCBI36
NG_015978.1:g.13942G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.484G>A MANE Select ENSP00000180166.5:p.Gly162Ser
ENST00000180166.5:c.484G>A ENSP00000180166.5:p.Gly162Ser
ENST00000519941.1:c.188G>A
NM_019851.2:c.484G>A NP_062825.1:p.Gly162Ser
NM_019851.3:c.484G>A MANE Select NP_062825.1:p.Gly162Ser
Search 100 bp 5'
Search 100 bp 3'