Canonical Allele Identifier: CA506113623
Gene: GDF15 HGNC NCBI

Linked Data

dbSNP Id: rs1971863608
MyVariant Identifiers: chr19:g.18499460C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18388650C>T , CM000681.2:g.18388650C>T GRCh38
NC_000019.9:g.18499460C>T , CM000681.1:g.18499460C>T GRCh37
NC_000019.8:g.18360460C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000595973.3:c.642C>T ENSP00000470531.3:p.His214=
ENST00000597765.2:c.642C>T ENSP00000469819.2:p.His214=
ENST00000252809.3:c.642C>T MANE Select ENSP00000252809.3:p.His214=
NM_004864.2:c.642C>T NP_004855.2:p.His214=
NM_004864.3:c.642C>T NP_004855.2:p.His214=
XM_024451789.1:c.642C>T XP_024307557.1:p.His214=
NM_004864.4:c.642C>T MANE Select NP_004855.2:p.His214=