Canonical Allele Identifier: CA2137041464

Gene: PTGER2

Linked Data

• dbSNP Id: rs2033898911

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.52321851_52321852del , CM000676.2:g.52321851_52321852del	GRCh38
NC_000014.8:g.52788569_52788570del , CM000676.1:g.52788569_52788570del	GRCh37
NC_000014.7:g.51858319_51858320del	NCBI36
NG_013082.1:g.12554_12555del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245457.6:c.844-5370_844-5369del MANE Select	ENSP00000245457.5:n.844-5370_844-5369del
ENST00000245457.5:c.844-5370_844-5369del	ENSP00000245457.5:n.844-5370_844-5369del
ENST00000557436.1:c.79-5370_79-5369del	ENSP00000450933.1:n.79-5370_79-5369del
NM_000956.3:c.844-5370_844-5369del	NP_000947.2:n.844-5370_844-5369del
NM_000956.4:c.844-5370_844-5369del MANE Select	NP_000947.2:n.844-5370_844-5369del