Canonical Allele Identifier: CA613904722
Gene: PTGER2 HGNC NCBI

Linked Data

dbSNP Id: rs1302058482
gnomAD v2: 14-52789140-CAA-C
gnomAD v3: 14-52322422-CAA-C
gnomAD v4: 14-52322422-CAA-C
MyVariant Identifiers: chr14:g.52789141_52789142del (hg19) chr14:g.52322423_52322424del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52322424_52322425del , CM000676.2:g.52322424_52322425del GRCh38
NC_000014.8:g.52789142_52789143del , CM000676.1:g.52789142_52789143del GRCh37
NC_000014.7:g.51858892_51858893del NCBI36
NG_013082.1:g.13127_13128del

Transcript Alleles

HGVS Amino-acid Change
ENST00000245457.6:c.844-4797_844-4796del MANE Select ENSP00000245457.5:n.844-4797_844-4796del
ENST00000245457.5:c.844-4797_844-4796del ENSP00000245457.5:n.844-4797_844-4796del
ENST00000557436.1:c.79-4797_79-4796del ENSP00000450933.1:n.79-4797_79-4796del
NM_000956.3:c.844-4797_844-4796del NP_000947.2:n.844-4797_844-4796del
NM_000956.4:c.844-4797_844-4796del MANE Select NP_000947.2:n.844-4797_844-4796del
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