Canonical Allele Identifier: CA404829628
Gene: GDF15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18499534T>C (hg19) chr19:g.18388724T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18388724T>C , CM000681.2:g.18388724T>C GRCh38
NC_000019.9:g.18499534T>C , CM000681.1:g.18499534T>C GRCh37
NC_000019.8:g.18360534T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000595973.3:c.716T>C ENSP00000470531.3:p.Met239Thr
ENST00000597765.2:c.716T>C ENSP00000469819.2:p.Met239Thr
ENST00000252809.3:c.716T>C MANE Select ENSP00000252809.3:p.Met239Thr
NM_004864.2:c.716T>C NP_004855.2:p.Met239Thr
NM_004864.3:c.716T>C NP_004855.2:p.Met239Thr
XM_024451789.1:c.716T>C XP_024307557.1:p.Met239Thr
NM_004864.4:c.716T>C MANE Select NP_004855.2:p.Met239Thr
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