Canonical Allele Identifier: CA2137042278
Gene: PTGER2 HGNC NCBI

Linked Data

dbSNP Id: rs1254590

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52322424A>T , CM000676.2:g.52322424A>T GRCh38
NC_000014.8:g.52789142A>T , CM000676.1:g.52789142A>T GRCh37
NC_000014.7:g.51858892A>T NCBI36
NG_013082.1:g.13127A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000245457.6:c.844-4797A>T MANE Select ENSP00000245457.5:n.844-4797A>T
ENST00000245457.5:c.844-4797A>T ENSP00000245457.5:n.844-4797A>T
ENST00000557436.1:c.79-4797A>T ENSP00000450933.1:n.79-4797A>T
NM_000956.3:c.844-4797A>T NP_000947.2:n.844-4797A>T
NM_000956.4:c.844-4797A>T MANE Select NP_000947.2:n.844-4797A>T