Canonical Allele Identifier: CA260917207
Gene: PTGER2 HGNC NCBI

Linked Data

dbSNP Id: rs764882813

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52322065G>T , CM000676.2:g.52322065G>T GRCh38
NC_000014.8:g.52788783G>T , CM000676.1:g.52788783G>T GRCh37
NC_000014.7:g.51858533G>T NCBI36
NG_013082.1:g.12768G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000245457.6:c.844-5156G>T MANE Select ENSP00000245457.5:n.844-5156G>T
ENST00000245457.5:c.844-5156G>T ENSP00000245457.5:n.844-5156G>T
ENST00000557436.1:c.79-5156G>T ENSP00000450933.1:n.79-5156G>T
NM_000956.3:c.844-5156G>T NP_000947.2:n.844-5156G>T
NM_000956.4:c.844-5156G>T MANE Select NP_000947.2:n.844-5156G>T