Canonical Allele Identifier: CA506113591
Gene: GDF15 HGNC NCBI

Linked Data

gnomAD v4: 19-18388602-C-A
MyVariant Identifiers: chr19:g.18499412C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18388602C>A , CM000681.2:g.18388602C>A GRCh38
NC_000019.9:g.18499412C>A , CM000681.1:g.18499412C>A GRCh37
NC_000019.8:g.18360412C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000595973.3:c.594C>A ENSP00000470531.3:p.Arg198=
ENST00000597765.2:c.594C>A ENSP00000469819.2:p.Arg198=
ENST00000252809.3:c.594C>A MANE Select ENSP00000252809.3:p.Arg198=
NM_004864.2:c.594C>A NP_004855.2:p.Arg198=
NM_004864.3:c.594C>A NP_004855.2:p.Arg198=
XM_024451789.1:c.594C>A XP_024307557.1:p.Arg198=
NM_004864.4:c.594C>A MANE Select NP_004855.2:p.Arg198=
Search 100 bp 5'
Search 100 bp 3'