Canonical Allele Identifier: CA527766484
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1175811679
gnomAD v2: 1-186649432-G-A
gnomAD v4: 1-186680300-G-A
MyVariant Identifiers: chr1:g.186649432G>A (hg19) chr1:g.186680300G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680300G>A , CM000663.2:g.186680300G>A GRCh38
NC_000001.10:g.186649432G>A , CM000663.1:g.186649432G>A GRCh37
NC_000001.9:g.184916055G>A NCBI36
NG_028206.2:g.5128C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.-10C>T MANE Select ENSP00000356438.5:n.-10C>T
ENST00000680451.1:c.-10C>T ENSP00000506242.1:n.-10C>T
ENST00000681605.1:c.-10C>T ENSP00000504900.1:n.-10C>T
ENST00000367468.9:c.-10C>T ENSP00000356438.5:n.-10C>T
ENST00000490885.6:n.124C>T
ENST00000559800.1:n.124C>T
NM_000963.3:c.-10C>T NP_000954.1:n.-10C>T
NM_000963.4:c.-10C>T MANE Select NP_000954.1:n.-10C>T
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