Canonical Allele Identifier: CA2366478866
Gene: MMP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011601A= , CM000682.2:g.46011601A= GRCh38
NC_000020.10:g.44640240A= , CM000682.1:g.44640240A= GRCh37
NC_000020.9:g.44073647A= NCBI36
NG_011468.1:g.7694A=

Transcript Alleles

HGVS Amino-acid change
ENST00000372330.3:c.851A= MANE Select ENSP00000361405.3:p.Asp284=
NM_004994.2:c.851A= NP_004985.2:p.Asp284=
NM_004994.3:c.851A= MANE Select NP_004985.2:p.Asp284=