Canonical Allele Identifier: CA506113626

Gene: GDF15

Linked Data

• MyVariant Identifiers: chr19:g.18499466C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18388656C>G , CM000681.2:g.18388656C>G	GRCh38
NC_000019.9:g.18499466C>G , CM000681.1:g.18499466C>G	GRCh37
NC_000019.8:g.18360466C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000595973.3:c.648C>G	ENSP00000470531.3:p.Val216=
ENST00000597765.2:c.648C>G	ENSP00000469819.2:p.Val216=
ENST00000252809.3:c.648C>G MANE Select	ENSP00000252809.3:p.Val216=
NM_004864.2:c.648C>G	NP_004855.2:p.Val216=
NM_004864.3:c.648C>G	NP_004855.2:p.Val216=
XM_024451789.1:c.648C>G	XP_024307557.1:p.Val216=
NM_004864.4:c.648C>G MANE Select	NP_004855.2:p.Val216=