Canonical Allele Identifier: CA506017606

Gene: GDF15

Linked Data

• gnomAD v4: 19-18388821-G-T
• MyVariant Identifiers: chr19:g.18499631G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18388821G>T , CM000681.2:g.18388821G>T	GRCh38
NC_000019.9:g.18499631G>T , CM000681.1:g.18499631G>T	GRCh37
NC_000019.8:g.18360631G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000595973.3:c.813G>T	ENSP00000470531.3:p.Ala271=
ENST00000597765.2:c.813G>T	ENSP00000469819.2:p.Ala271=
ENST00000252809.3:c.813G>T MANE Select	ENSP00000252809.3:p.Ala271=
NM_004864.2:c.813G>T	NP_004855.2:p.Ala271=
NM_004864.3:c.813G>T	NP_004855.2:p.Ala271=
XM_024451789.1:c.813G>T	XP_024307557.1:p.Ala271=
NM_004864.4:c.813G>T MANE Select	NP_004855.2:p.Ala271=