Canonical Allele Identifier: CA260917082
Gene: PTGER2 HGNC NCBI

Linked Data

dbSNP Id: rs546308670
gnomAD v3: 14-52321916-C-T
gnomAD v4: 14-52321916-C-T
MyVariant Identifiers: chr14:g.52788634C>T (hg19) chr14:g.52321916C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52321916C>T , CM000676.2:g.52321916C>T GRCh38
NC_000014.8:g.52788634C>T , CM000676.1:g.52788634C>T GRCh37
NC_000014.7:g.51858384C>T NCBI36
NG_013082.1:g.12619C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000245457.6:c.844-5305C>T MANE Select ENSP00000245457.5:n.844-5305C>T
ENST00000245457.5:c.844-5305C>T ENSP00000245457.5:n.844-5305C>T
ENST00000557436.1:c.79-5305C>T ENSP00000450933.1:n.79-5305C>T
NM_000956.3:c.844-5305C>T NP_000947.2:n.844-5305C>T
NM_000956.4:c.844-5305C>T MANE Select NP_000947.2:n.844-5305C>T
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