Canonical Allele Identifier: CA2366478592
Gene: MMP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011054A= , CM000682.2:g.46011054A= GRCh38
NC_000020.10:g.44639693A= , CM000682.1:g.44639693A= GRCh37
NC_000020.9:g.44073100A= NCBI36
NG_011468.1:g.7147A=

Transcript Alleles

HGVS Amino-acid change
ENST00000372330.3:c.649+4A= MANE Select ENSP00000361405.3:n.649+4A=
NM_004994.2:c.649+4A= NP_004985.2:n.649+4A=
NM_004994.3:c.649+4A= MANE Select NP_004985.2:n.649+4A=