Canonical Allele Identifier: CA2366478597
Gene: MMP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011068C= , CM000682.2:g.46011068C= GRCh38
NC_000020.10:g.44639707C= , CM000682.1:g.44639707C= GRCh37
NC_000020.9:g.44073114C= NCBI36
NG_011468.1:g.7161C=

Transcript Alleles

HGVS Amino-acid change
ENST00000372330.3:c.649+18C= MANE Select ENSP00000361405.3:n.649+18C=
NM_004994.2:c.649+18C= NP_004985.2:n.649+18C=
NM_004994.3:c.649+18C= MANE Select NP_004985.2:n.649+18C=