Canonical Allele Identifier: CA404830134
Gene: GDF15 HGNC NCBI

Linked Data

dbSNP Id: rs1160695990
gnomAD v2: 19-18499599-C-G
gnomAD v4: 19-18388789-C-G
MyVariant Identifiers: chr19:g.18499599C>G (hg19) chr19:g.18388789C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18388789C>G , CM000681.2:g.18388789C>G GRCh38
NC_000019.9:g.18499599C>G , CM000681.1:g.18499599C>G GRCh37
NC_000019.8:g.18360599C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000595973.3:c.781C>G ENSP00000470531.3:p.Leu261Val
ENST00000597765.2:c.781C>G ENSP00000469819.2:p.Leu261Val
ENST00000252809.3:c.781C>G MANE Select ENSP00000252809.3:p.Leu261Val
NM_004864.2:c.781C>G NP_004855.2:p.Leu261Val
NM_004864.3:c.781C>G NP_004855.2:p.Leu261Val
XM_024451789.1:c.781C>G XP_024307557.1:p.Leu261Val
NM_004864.4:c.781C>G MANE Select NP_004855.2:p.Leu261Val
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