Canonical Allele Identifier: CA34081660
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs561009903
gnomAD v3: 1-186672661-G-A
gnomAD v4: 1-186672661-G-A
MyVariant Identifiers: chr1:g.186641793G>A (hg19) chr1:g.186672661G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186672661G>A , CM000663.2:g.186672661G>A GRCh38
NC_000001.10:g.186641793G>A , CM000663.1:g.186641793G>A GRCh37
NC_000001.9:g.184908416G>A NCBI36
NG_028206.2:g.12767C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000367468.10:c.*1692C>T MANE Select ENSP00000356438.5:n.*1692C>T
ENST00000680451.1:c.*1692C>T ENSP00000506242.1:n.*1692C>T
ENST00000681605.1:c.*3179C>T ENSP00000504900.1:n.*3179C>T
ENST00000367468.9:c.*1692C>T ENSP00000356438.5:n.*1692C>T
NM_000963.3:c.*1692C>T NP_000954.1:n.*1692C>T
NM_000963.4:c.*1692C>T MANE Select NP_000954.1:n.*1692C>T
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