Canonical Allele Identifier: CA2137041858
Gene: PTGER2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52322139A= , CM000676.2:g.52322139A= GRCh38
NC_000014.8:g.52788857A= , CM000676.1:g.52788857A= GRCh37
NC_000014.7:g.51858607A= NCBI36
NG_013082.1:g.12842A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000245457.6:c.844-5082A= MANE Select ENSP00000245457.5:n.844-5082A=
ENST00000245457.5:c.844-5082A= ENSP00000245457.5:n.844-5082A=
ENST00000557436.1:c.79-5082A= ENSP00000450933.1:n.79-5082A=
NM_000956.3:c.844-5082A= NP_000947.2:n.844-5082A=
NM_000956.4:c.844-5082A= MANE Select NP_000947.2:n.844-5082A=