Canonical Allele Identifier: CA963156470

Gene: PTGER2

Linked Data

• dbSNP Id: rs2033901424
• gnomAD v3: 14-52322072-CTAAT-C
• gnomAD v4: 14-52322072-CTAAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.52322076_52322079del , CM000676.2:g.52322076_52322079del	GRCh38
NC_000014.8:g.52788794_52788797del , CM000676.1:g.52788794_52788797del	GRCh37
NC_000014.7:g.51858544_51858547del	NCBI36
NG_013082.1:g.12779_12782del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245457.6:c.844-5145_844-5142del MANE Select	ENSP00000245457.5:n.844-5145_844-5142del
ENST00000245457.5:c.844-5145_844-5142del	ENSP00000245457.5:n.844-5145_844-5142del
ENST00000557436.1:c.79-5145_79-5142del	ENSP00000450933.1:n.79-5145_79-5142del
NM_000956.3:c.844-5145_844-5142del	NP_000947.2:n.844-5145_844-5142del
NM_000956.4:c.844-5145_844-5142del MANE Select	NP_000947.2:n.844-5145_844-5142del