Canonical Allele Identifier: CA404830348
Gene: GDF15 HGNC NCBI

Linked Data

ClinVar Variation Id: 2225389
ClinVar RCV Id: RCV004084646
dbSNP Id: rs759715270

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18388831G>C , CM000681.2:g.18388831G>C GRCh38
NC_000019.9:g.18499641G>C , CM000681.1:g.18499641G>C GRCh37
NC_000019.8:g.18360641G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000595973.3:c.823G>C ENSP00000470531.3:p.Val275Leu
ENST00000597765.2:c.823G>C ENSP00000469819.2:p.Val275Leu
ENST00000252809.3:c.823G>C MANE Select ENSP00000252809.3:p.Val275Leu
NM_004864.2:c.823G>C NP_004855.2:p.Val275Leu
NM_004864.3:c.823G>C NP_004855.2:p.Val275Leu
XM_024451789.1:c.823G>C XP_024307557.1:p.Val275Leu
NM_004864.4:c.823G>C MANE Select NP_004855.2:p.Val275Leu