Canonical Allele Identifier: CA13383734
Gene: PTGDR2 HGNC NCBI
MyVariant.info:
GRCh38 chr11:g.60852184T>C
GRCh37 chr11:g.60619657T>C
gnomAD v2:
11:60619657 T / C
gnomAD v3:
11:60852184 T / C
gnomAD v4:
chr11-60852184-T-C
Joint Max Group AF 0.69642978 (EAS)
Genomes Max Group AF 0.71321924 (EAS)
Exomes Max Group AF 0.67906277 (EAS)
dbSNP:
545659
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.60852184T>C , CM000673.2:g.60852184T>C GRCh38
NC_000011.9:g.60619657T>C , CM000673.1:g.60619657T>C GRCh37
NC_000011.8:g.60376233T>C NCBI36
NG_016170.1:g.8788A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000332539.5:c.*351A>G MANE Select ENSP00000332812.4:n.*351A>G
ENST00000332539.4:c.*351A>G ENSP00000332812.4:n.*351A>G
NM_004778.2:c.*351A>G NP_004769.2:n.*351A>G
NM_004778.3:c.*351A>G MANE Select NP_004769.2:n.*351A>G
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