Canonical Allele Identifier: CA613904725
Gene: PTGER2 HGNC NCBI

Linked Data

dbSNP Id: rs1220641795
gnomAD v2: 14-52789144-GATCACAAGGCAAAGGGCAAAAGCAA-G
gnomAD v3: 14-52322426-GATCACAAGGCAAAGGGCAAAAGCAA-G
gnomAD v4: 14-52322426-GATCACAAGGCAAAGGGCAAAAGCAA-G
MyVariant Identifiers: chr14:g.52789145_52789169del (hg19) chr14:g.52322427_52322451del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52322428_52322452del , CM000676.2:g.52322428_52322452del GRCh38
NC_000014.8:g.52789146_52789170del , CM000676.1:g.52789146_52789170del GRCh37
NC_000014.7:g.51858896_51858920del NCBI36
NG_013082.1:g.13131_13155del

Transcript Alleles

HGVS Amino-acid Change
ENST00000245457.6:c.844-4793_844-4769del MANE Select ENSP00000245457.5:n.844-4793_844-4769del
ENST00000245457.5:c.844-4793_844-4769del ENSP00000245457.5:n.844-4793_844-4769del
ENST00000557436.1:c.79-4793_79-4769del ENSP00000450933.1:n.79-4793_79-4769del
NM_000956.3:c.844-4793_844-4769del NP_000947.2:n.844-4793_844-4769del
NM_000956.4:c.844-4793_844-4769del MANE Select NP_000947.2:n.844-4793_844-4769del
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