Canonical Allele Identifier: CA506113710
Gene: GDF15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18499571A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18388761A>G , CM000681.2:g.18388761A>G GRCh38
NC_000019.9:g.18499571A>G , CM000681.1:g.18499571A>G GRCh37
NC_000019.8:g.18360571A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000595973.3:c.753A>G ENSP00000470531.3:p.Ala251=
ENST00000597765.2:c.753A>G ENSP00000469819.2:p.Ala251=
ENST00000252809.3:c.753A>G MANE Select ENSP00000252809.3:p.Ala251=
NM_004864.2:c.753A>G NP_004855.2:p.Ala251=
NM_004864.3:c.753A>G NP_004855.2:p.Ala251=
XM_024451789.1:c.753A>G XP_024307557.1:p.Ala251=
NM_004864.4:c.753A>G MANE Select NP_004855.2:p.Ala251=