Canonical Allele Identifier: CA2366478637
Gene: MMP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011138T= , CM000682.2:g.46011138T= GRCh38
NC_000020.10:g.44639777T= , CM000682.1:g.44639777T= GRCh37
NC_000020.9:g.44073184T= NCBI36
NG_011468.1:g.7231T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.650-5T= MANE Select ENSP00000361405.3:n.650-5T=
NM_004994.2:c.650-5T= NP_004985.2:n.650-5T=
NM_004994.3:c.650-5T= MANE Select NP_004985.2:n.650-5T=