Canonical Allele Identifier: CA9557881
Gene: FGF21 HGNC NCBI
MyVariant.info:
GRCh38 chr19:g.48756272A>G
GRCh37 chr19:g.49259529A>G
gnomAD v2:
19:49259529 A / G
gnomAD v3:
19:48756272 A / G
gnomAD v4:
chr19-48756272-A-G
Joint Max Group AF 0.98536025 (EAS)
Genomes Max Group AF 0.97149155 (EAS)
Exomes Max Group AF 0.98472934 (EAS)
dbSNP:
838133
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48756272A>G , CM000681.2:g.48756272A>G GRCh38
NC_000019.9:g.49259529A>G , CM000681.1:g.49259529A>G GRCh37
NC_000019.8:g.53951341A>G NCBI36
NG_007510.1:g.4119T>C
NG_033945.1:g.5186A>G
NG_007510.2:g.4119T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000222157.5:c.36A>G ENSP00000222157.3:p.Gly12=
ENST00000593756.6:c.36A>G MANE Select ENSP00000471477.1:p.Gly12=
ENST00000222157.4:c.36A>G ENSP00000222157.3:p.Gly12=
ENST00000593756.5:c.36A>G ENSP00000471477.1:p.Gly12=
NM_019113.2:c.36A>G NP_061986.1:p.Gly12=
XM_005258731.1:c.36A>G XP_005258788.1:p.Gly12=
NM_019113.3:c.36A>G NP_061986.1:p.Gly12=
NM_019113.4:c.36A>G MANE Select NP_061986.1:p.Gly12=
Search 100 bp 5'
Search 100 bp 3'