Canonical Allele Identifier: CA2366478867
Gene: MMP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011605G= , CM000682.2:g.46011605G= GRCh38
NC_000020.10:g.44640244G= , CM000682.1:g.44640244G= GRCh37
NC_000020.9:g.44073651G= NCBI36
NG_011468.1:g.7698G=

Transcript Alleles

HGVS Amino-acid change
ENST00000372330.3:c.855G= MANE Select ENSP00000361405.3:p.Gly285=
NM_004994.2:c.855G= NP_004985.2:p.Gly285=
NM_004994.3:c.855G= MANE Select NP_004985.2:p.Gly285=