Canonical Allele Identifier: CA404829876
Gene: GDF15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18499560T>A (hg19) chr19:g.18388750T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18388750T>A , CM000681.2:g.18388750T>A GRCh38
NC_000019.9:g.18499560T>A , CM000681.1:g.18499560T>A GRCh37
NC_000019.8:g.18360560T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000595973.3:c.742T>A ENSP00000470531.3:p.Phe248Ile
ENST00000597765.2:c.742T>A ENSP00000469819.2:p.Phe248Ile
ENST00000252809.3:c.742T>A MANE Select ENSP00000252809.3:p.Phe248Ile
NM_004864.2:c.742T>A NP_004855.2:p.Phe248Ile
NM_004864.3:c.742T>A NP_004855.2:p.Phe248Ile
XM_024451789.1:c.742T>A XP_024307557.1:p.Phe248Ile
NM_004864.4:c.742T>A MANE Select NP_004855.2:p.Phe248Ile
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