Canonical Allele Identifier: CA506113647
Gene: GDF15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18499490C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18388680C>A , CM000681.2:g.18388680C>A GRCh38
NC_000019.9:g.18499490C>A , CM000681.1:g.18499490C>A GRCh37
NC_000019.8:g.18360490C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000595973.3:c.672C>A ENSP00000470531.3:p.Gly224=
ENST00000597765.2:c.672C>A ENSP00000469819.2:p.Gly224=
ENST00000252809.3:c.672C>A MANE Select ENSP00000252809.3:p.Gly224=
NM_004864.2:c.672C>A NP_004855.2:p.Gly224=
NM_004864.3:c.672C>A NP_004855.2:p.Gly224=
XM_024451789.1:c.672C>A XP_024307557.1:p.Gly224=
NM_004864.4:c.672C>A MANE Select NP_004855.2:p.Gly224=
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