Canonical Allele Identifier: CA422374013
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.186649895A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680763A>C , CM000663.2:g.186680763A>C GRCh38
NC_000001.10:g.186649895A>C , CM000663.1:g.186649895A>C GRCh37
NC_000001.9:g.184916518A>C NCBI36
NG_028206.2:g.4665T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-173T>G (PTGS2) ENSP00000506242.1:n.-173T>G
NR_125801.1:n.110A>C (PACERR)
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