Canonical Allele Identifier: CA2729739628

Gene: PTGER2

Linked Data

• dbSNP Id: rs2140038037

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.52321907_52321910del , CM000676.2:g.52321907_52321910del	GRCh38
NC_000014.8:g.52788625_52788628del , CM000676.1:g.52788625_52788628del	GRCh37
NC_000014.7:g.51858375_51858378del	NCBI36
NG_013082.1:g.12610_12613del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245457.6:c.844-5314_844-5311del MANE Select	ENSP00000245457.5:n.844-5314_844-5311del
ENST00000245457.5:c.844-5314_844-5311del	ENSP00000245457.5:n.844-5314_844-5311del
ENST00000557436.1:c.79-5314_79-5311del	ENSP00000450933.1:n.79-5314_79-5311del
NM_000956.3:c.844-5314_844-5311del	NP_000947.2:n.844-5314_844-5311del
NM_000956.4:c.844-5314_844-5311del MANE Select	NP_000947.2:n.844-5314_844-5311del