Canonical Allele Identifier: CA9310774
Gene: GDF15 HGNC NCBI

Linked Data

dbSNP Id: rs767853331
ExAC: 19:18499394 C / G
gnomAD v2: 19-18499394-C-G
gnomAD v3: 19-18388584-C-G
gnomAD v4: 19-18388584-C-G
MyVariant Identifiers: chr19:g.18499394C>G (hg19) chr19:g.18388584C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18388584C>G , CM000681.2:g.18388584C>G GRCh38
NC_000019.9:g.18499394C>G , CM000681.1:g.18499394C>G GRCh37
NC_000019.8:g.18360394C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000595973.3:c.576C>G ENSP00000470531.3:p.Arg192=
ENST00000597765.2:c.576C>G ENSP00000469819.2:p.Arg192=
ENST00000252809.3:c.576C>G MANE Select ENSP00000252809.3:p.Arg192=
NM_004864.2:c.576C>G NP_004855.2:p.Arg192=
NM_004864.3:c.576C>G NP_004855.2:p.Arg192=
XM_024451789.1:c.576C>G XP_024307557.1:p.Arg192=
NM_004864.4:c.576C>G MANE Select NP_004855.2:p.Arg192=
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