Canonical Allele Identifier: CA260917402
Gene: PTGER2 HGNC NCBI

Linked Data

dbSNP Id: rs200403853
gnomAD v2: 14-52788984-CA-C
gnomAD v3: 14-52322266-CA-C
gnomAD v4: 14-52322266-CA-C
MyVariant Identifiers: chr14:g.52788985del (hg19) chr14:g.52322267del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52322267del , CM000676.2:g.52322267del GRCh38
NC_000014.8:g.52788985del , CM000676.1:g.52788985del GRCh37
NC_000014.7:g.51858735del NCBI36
NG_013082.1:g.12970del

Transcript Alleles

HGVS Amino-acid Change
ENST00000245457.6:c.844-4954del MANE Select ENSP00000245457.5:n.844-4954del
ENST00000245457.5:c.844-4954del ENSP00000245457.5:n.844-4954del
ENST00000557436.1:c.79-4954del ENSP00000450933.1:n.79-4954del
NM_000956.3:c.844-4954del NP_000947.2:n.844-4954del
NM_000956.4:c.844-4954del MANE Select NP_000947.2:n.844-4954del
Search 100 bp 5'
Search 100 bp 3'