Canonical Allele Identifier: CA260917065
Gene: PTGER2 HGNC NCBI

Linked Data

dbSNP Id: rs777850879
MyVariant Identifiers: chr14:g.52788590T>C (hg19) chr14:g.52321872T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52321872T>C , CM000676.2:g.52321872T>C GRCh38
NC_000014.8:g.52788590T>C , CM000676.1:g.52788590T>C GRCh37
NC_000014.7:g.51858340T>C NCBI36
NG_013082.1:g.12575T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000245457.6:c.844-5349T>C MANE Select ENSP00000245457.5:n.844-5349T>C
ENST00000245457.5:c.844-5349T>C ENSP00000245457.5:n.844-5349T>C
ENST00000557436.1:c.79-5349T>C ENSP00000450933.1:n.79-5349T>C
NM_000956.3:c.844-5349T>C NP_000947.2:n.844-5349T>C
NM_000956.4:c.844-5349T>C MANE Select NP_000947.2:n.844-5349T>C
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