Canonical Allele Identifier: CA2816507483
Gene: MMP9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011786T>A , CM000682.2:g.46011786T>A GRCh38
NC_000020.10:g.44640425T>A , CM000682.1:g.44640425T>A GRCh37
NC_000020.9:g.44073832T>A NCBI36
NG_011468.1:g.7879T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.997+39T>A MANE Select ENSP00000361405.3:n.997+39T>A
NM_004994.2:c.997+39T>A NP_004985.2:n.997+39T>A
NM_004994.3:c.997+39T>A MANE Select NP_004985.2:n.997+39T>A
Search 100 bp 5'
Search 100 bp 3'