Canonical Allele Identifier: CA404829992
Gene: GDF15 HGNC NCBI

Linked Data

gnomAD v4: 19-18388766-T-C
COSMIC: COSM311429
MyVariant Identifiers: chr19:g.18499576T>C (hg19) chr19:g.18388766T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18388766T>C , CM000681.2:g.18388766T>C GRCh38
NC_000019.9:g.18499576T>C , CM000681.1:g.18499576T>C GRCh37
NC_000019.8:g.18360576T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000595973.3:c.758T>C ENSP00000470531.3:p.Met253Thr
ENST00000597765.2:c.758T>C ENSP00000469819.2:p.Met253Thr
ENST00000252809.3:c.758T>C MANE Select ENSP00000252809.3:p.Met253Thr
NM_004864.2:c.758T>C NP_004855.2:p.Met253Thr
NM_004864.3:c.758T>C NP_004855.2:p.Met253Thr
XM_024451789.1:c.758T>C XP_024307557.1:p.Met253Thr
NM_004864.4:c.758T>C MANE Select NP_004855.2:p.Met253Thr
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