Canonical Allele Identifier: CA728763366
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs200278253
MyVariant Identifiers: chr1:g.186649473C>G (hg19) chr1:g.186680341C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680341C>G , CM000663.2:g.186680341C>G GRCh38
NC_000001.10:g.186649473C>G , CM000663.1:g.186649473C>G GRCh37
NC_000001.9:g.184916096C>G NCBI36
NG_028206.2:g.5087G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.-51G>C MANE Select ENSP00000356438.5:n.-51G>C
ENST00000680451.1:c.-51G>C ENSP00000506242.1:n.-51G>C
ENST00000681605.1:c.-51G>C ENSP00000504900.1:n.-51G>C
ENST00000367468.9:c.-51G>C ENSP00000356438.5:n.-51G>C
ENST00000490885.6:n.83G>C
ENST00000559800.1:n.83G>C
NM_000963.3:c.-51G>C NP_000954.1:n.-51G>C
NM_000963.4:c.-51G>C MANE Select NP_000954.1:n.-51G>C
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