Canonical Allele Identifier: CA2366478598
Gene: MMP9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011071G= , CM000682.2:g.46011071G= GRCh38
NC_000020.10:g.44639710G= , CM000682.1:g.44639710G= GRCh37
NC_000020.9:g.44073117G= NCBI36
NG_011468.1:g.7164G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.649+21G= MANE Select ENSP00000361405.3:n.649+21G=
NM_004994.2:c.649+21G= NP_004985.2:n.649+21G=
NM_004994.3:c.649+21G= MANE Select NP_004985.2:n.649+21G=
Search 100 bp 5'
Search 100 bp 3'