Canonical Allele Identifier: CA506017658
Gene: GDF15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18499673T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18388863T>A , CM000681.2:g.18388863T>A GRCh38
NC_000019.9:g.18499673T>A , CM000681.1:g.18499673T>A GRCh37
NC_000019.8:g.18360673T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000595973.3:c.855T>A ENSP00000470531.3:p.Ile285=
ENST00000597765.2:c.855T>A ENSP00000469819.2:p.Ile285=
ENST00000252809.3:c.855T>A MANE Select ENSP00000252809.3:p.Ile285=
NM_004864.2:c.855T>A NP_004855.2:p.Ile285=
NM_004864.3:c.855T>A NP_004855.2:p.Ile285=
XM_024451789.1:c.855T>A XP_024307557.1:p.Ile285=
NM_004864.4:c.855T>A MANE Select NP_004855.2:p.Ile285=