Canonical Allele Identifier: CA2649583182
Gene: PTGS2 HGNC NCBI

Linked Data

gnomAD v4: 1-186680334-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680334C>A , CM000663.2:g.186680334C>A GRCh38
NC_000001.10:g.186649466C>A , CM000663.1:g.186649466C>A GRCh37
NC_000001.9:g.184916089C>A NCBI36
NG_028206.2:g.5094G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.-44G>T MANE Select ENSP00000356438.5:n.-44G>T
ENST00000680451.1:c.-44G>T ENSP00000506242.1:n.-44G>T
ENST00000681605.1:c.-44G>T ENSP00000504900.1:n.-44G>T
ENST00000367468.9:c.-44G>T ENSP00000356438.5:n.-44G>T
ENST00000490885.6:n.90G>T
ENST00000559800.1:n.90G>T
NM_000963.3:c.-44G>T NP_000954.1:n.-44G>T
NM_000963.4:c.-44G>T MANE Select NP_000954.1:n.-44G>T
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