Canonical Allele Identifier: CA2137057937
Gene: PTGDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52274253A>T , CM000676.2:g.52274253A>T GRCh38
NC_000014.8:g.52740971A>T , CM000676.1:g.52740971A>T GRCh37
NC_000014.7:g.51810721A>T NCBI36
NG_012118.1:g.11541A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000306051.3:c.847-478A>T MANE Select ENSP00000303424.2:n.847-478A>T
ENST00000306051.2:c.847-478A>T ENSP00000303424.2:n.847-478A>T
ENST00000553372.1:c.*47-478A>T ENSP00000452408.1:n.*47-478A>T
NM_000953.2:c.847-478A>T NP_000944.1:n.847-478A>T
NM_001281469.1:c.*47-478A>T NP_001268398.1:n.*47-478A>T
XM_005267891.2:c.847-478A>T XP_005267948.1:n.847-478A>T
XM_005267891.4:c.847-478A>T XP_005267948.1:n.847-478A>T
NM_000953.3:c.847-478A>T MANE Select NP_000944.1:n.847-478A>T
NM_001281469.2:c.*47-478A>T NP_001268398.1:n.*47-478A>T