Canonical Allele Identifier: CA9310812
Gene: GDF15 HGNC NCBI

Linked Data

ClinVar Variation Id: 3099242
ClinVar RCV Id: RCV004387588
dbSNP Id: rs766507873
ExAC: 19:18499525 A / G
gnomAD v2: 19-18499525-A-G
gnomAD v3: 19-18388715-A-G
gnomAD v4: 19-18388715-A-G
MyVariant Identifiers: chr19:g.18499525A>G (hg19) chr19:g.18388715A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18388715A>G , CM000681.2:g.18388715A>G GRCh38
NC_000019.9:g.18499525A>G , CM000681.1:g.18499525A>G GRCh37
NC_000019.8:g.18360525A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000595973.3:c.707A>G ENSP00000470531.3:p.Gln236Arg
ENST00000597765.2:c.707A>G ENSP00000469819.2:p.Gln236Arg
ENST00000252809.3:c.707A>G MANE Select ENSP00000252809.3:p.Gln236Arg
NM_004864.2:c.707A>G NP_004855.2:p.Gln236Arg
NM_004864.3:c.707A>G NP_004855.2:p.Gln236Arg
XM_024451789.1:c.707A>G XP_024307557.1:p.Gln236Arg
NM_004864.4:c.707A>G MANE Select NP_004855.2:p.Gln236Arg
Search 100 bp 5'
Search 100 bp 3'