Canonical Allele Identifier: CA1213245369
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1665843257
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186679753T>A , CM000663.2:g.186679753T>A GRCh38
NC_000001.10:g.186648885T>A , CM000663.1:g.186648885T>A GRCh37
NC_000001.9:g.184915508T>A NCBI36
NG_028206.2:g.5675A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000367468.10:c.53-315A>T MANE Select ENSP00000356438.5:n.53-315A>T
ENST00000680451.1:c.53-315A>T ENSP00000506242.1:n.53-315A>T
ENST00000681605.1:c.53-315A>T ENSP00000504900.1:n.53-315A>T
ENST00000367468.9:c.53-315A>T ENSP00000356438.5:n.53-315A>T
ENST00000490885.6:n.186-315A>T
ENST00000559627.1:c.53-315A>T ENSP00000454130.1:n.53-315A>T
ENST00000559800.1:n.186-315A>T
NM_000963.3:c.53-315A>T NP_000954.1:n.53-315A>T
NM_000963.4:c.53-315A>T MANE Select NP_000954.1:n.53-315A>T
Search 100 bp 5'
Search 100 bp 3'