Canonical Allele Identifier: CA260917162
Gene: PTGER2 HGNC NCBI

Linked Data

dbSNP Id: rs959950675
gnomAD v3: 14-52322008-C-A
gnomAD v4: 14-52322008-C-A
MyVariant Identifiers: chr14:g.52788726C>A (hg19) chr14:g.52322008C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52322008C>A , CM000676.2:g.52322008C>A GRCh38
NC_000014.8:g.52788726C>A , CM000676.1:g.52788726C>A GRCh37
NC_000014.7:g.51858476C>A NCBI36
NG_013082.1:g.12711C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000245457.6:c.844-5213C>A MANE Select ENSP00000245457.5:n.844-5213C>A
ENST00000245457.5:c.844-5213C>A ENSP00000245457.5:n.844-5213C>A
ENST00000557436.1:c.79-5213C>A ENSP00000450933.1:n.79-5213C>A
NM_000956.3:c.844-5213C>A NP_000947.2:n.844-5213C>A
NM_000956.4:c.844-5213C>A MANE Select NP_000947.2:n.844-5213C>A
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