Canonical Allele Identifier: CA728758680
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1173888940
MyVariant Identifiers: chr1:g.186643016A>C (hg19) chr1:g.186673884A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673884A>C , CM000663.2:g.186673884A>C GRCh38
NC_000001.10:g.186643016A>C , CM000663.1:g.186643016A>C GRCh37
NC_000001.9:g.184909639A>C NCBI36
NG_028206.2:g.11544T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.*469T>G MANE Select ENSP00000356438.5:n.*469T>G
ENST00000680451.1:c.*469T>G ENSP00000506242.1:n.*469T>G
ENST00000681605.1:c.*1956T>G ENSP00000504900.1:n.*1956T>G
ENST00000367468.9:c.*469T>G ENSP00000356438.5:n.*469T>G
ENST00000490885.6:n.2699T>G
NM_000963.3:c.*469T>G NP_000954.1:n.*469T>G
NM_000963.4:c.*469T>G MANE Select NP_000954.1:n.*469T>G
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