Canonical Allele Identifier: CA506113685
Gene: GDF15 HGNC NCBI

Linked Data

dbSNP Id: rs1303218550
gnomAD v2: 19-18499547-G-A
gnomAD v3: 19-18388737-G-A
gnomAD v4: 19-18388737-G-A
MyVariant Identifiers: chr19:g.18499547G>A (hg19) chr19:g.18388737G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18388737G>A , CM000681.2:g.18388737G>A GRCh38
NC_000019.9:g.18499547G>A , CM000681.1:g.18499547G>A GRCh37
NC_000019.8:g.18360547G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000595973.3:c.729G>A ENSP00000470531.3:p.Ala243=
ENST00000597765.2:c.729G>A ENSP00000469819.2:p.Ala243=
ENST00000252809.3:c.729G>A MANE Select ENSP00000252809.3:p.Ala243=
NM_004864.2:c.729G>A NP_004855.2:p.Ala243=
NM_004864.3:c.729G>A NP_004855.2:p.Ala243=
XM_024451789.1:c.729G>A XP_024307557.1:p.Ala243=
NM_004864.4:c.729G>A MANE Select NP_004855.2:p.Ala243=
Search 100 bp 5'
Search 100 bp 3'