Canonical Allele Identifier: CA2366478868
Gene: MMP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011608A= , CM000682.2:g.46011608A= GRCh38
NC_000020.10:g.44640247A= , CM000682.1:g.44640247A= GRCh37
NC_000020.9:g.44073654A= NCBI36
NG_011468.1:g.7701A=

Transcript Alleles

HGVS Amino-acid change
ENST00000372330.3:c.858A= MANE Select ENSP00000361405.3:p.Lys286=
NM_004994.2:c.858A= NP_004985.2:p.Lys286=
NM_004994.3:c.858A= MANE Select NP_004985.2:p.Lys286=