Canonical Allele Identifier: CA2366478822
Gene: MMP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011525A= , CM000682.2:g.46011525A= GRCh38
NC_000020.10:g.44640164A= , CM000682.1:g.44640164A= GRCh37
NC_000020.9:g.44073571A= NCBI36
NG_011468.1:g.7618A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.824-49A= MANE Select ENSP00000361405.3:n.824-49A=
NM_004994.2:c.824-49A= NP_004985.2:n.824-49A=
NM_004994.3:c.824-49A= MANE Select NP_004985.2:n.824-49A=