Canonical Allele Identifier: CA963156398
Gene: PTGER2 HGNC NCBI

Linked Data

dbSNP Id: rs2033899063

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52321864_52321865del , CM000676.2:g.52321864_52321865del GRCh38
NC_000014.8:g.52788582_52788583del , CM000676.1:g.52788582_52788583del GRCh37
NC_000014.7:g.51858332_51858333del NCBI36
NG_013082.1:g.12567_12568del

Transcript Alleles

HGVS Amino-acid Change
ENST00000245457.6:c.844-5357_844-5356del MANE Select ENSP00000245457.5:n.844-5357_844-5356del
ENST00000245457.5:c.844-5357_844-5356del ENSP00000245457.5:n.844-5357_844-5356del
ENST00000557436.1:c.79-5357_79-5356del ENSP00000450933.1:n.79-5357_79-5356del
NM_000956.3:c.844-5357_844-5356del NP_000947.2:n.844-5357_844-5356del
NM_000956.4:c.844-5357_844-5356del MANE Select NP_000947.2:n.844-5357_844-5356del