Canonical Allele Identifier: CA2366478562
Gene: MMP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46010973C= , CM000682.2:g.46010973C= GRCh38
NC_000020.10:g.44639612C= , CM000682.1:g.44639612C= GRCh37
NC_000020.9:g.44073019C= NCBI36
NG_011468.1:g.7066C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.572C= MANE Select ENSP00000361405.3:p.Ala191=
NM_004994.2:c.572C= NP_004985.2:p.Ala191=
NM_004994.3:c.572C= MANE Select NP_004985.2:p.Ala191=