Canonical Allele Identifier: CA34082328
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs916982210
MyVariant Identifiers: chr1:g.186648787C>T (hg19) chr1:g.186679655C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186679655C>T , CM000663.2:g.186679655C>T GRCh38
NC_000001.10:g.186648787C>T , CM000663.1:g.186648787C>T GRCh37
NC_000001.9:g.184915410C>T NCBI36
NG_028206.2:g.5773G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000367468.10:c.53-217G>A MANE Select ENSP00000356438.5:n.53-217G>A
ENST00000680451.1:c.53-217G>A ENSP00000506242.1:n.53-217G>A
ENST00000681605.1:c.53-217G>A ENSP00000504900.1:n.53-217G>A
ENST00000367468.9:c.53-217G>A ENSP00000356438.5:n.53-217G>A
ENST00000490885.6:n.186-217G>A
ENST00000559627.1:c.53-217G>A ENSP00000454130.1:n.53-217G>A
ENST00000559800.1:n.186-217G>A
NM_000963.3:c.53-217G>A NP_000954.1:n.53-217G>A
NM_000963.4:c.53-217G>A MANE Select NP_000954.1:n.53-217G>A
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