Canonical Allele Identifier: CA404828139
Gene: GDF15 HGNC NCBI

Linked Data

dbSNP Id: rs770559920
gnomAD v2: 19-18499375-C-G
gnomAD v4: 19-18388565-C-G
MyVariant Identifiers: chr19:g.18499375C>G (hg19) chr19:g.18388565C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18388565C>G , CM000681.2:g.18388565C>G GRCh38
NC_000019.9:g.18499375C>G , CM000681.1:g.18499375C>G GRCh37
NC_000019.8:g.18360375C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000595973.3:c.557C>G ENSP00000470531.3:p.Pro186Arg
ENST00000597765.2:c.557C>G ENSP00000469819.2:p.Pro186Arg
ENST00000252809.3:c.557C>G MANE Select ENSP00000252809.3:p.Pro186Arg
NM_004864.2:c.557C>G NP_004855.2:p.Pro186Arg
NM_004864.3:c.557C>G NP_004855.2:p.Pro186Arg
XM_024451789.1:c.557C>G XP_024307557.1:p.Pro186Arg
NM_004864.4:c.557C>G MANE Select NP_004855.2:p.Pro186Arg
Search 100 bp 5'
Search 100 bp 3'