Canonical Allele Identifier: CA2366478537
Gene: MMP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46010935G= , CM000682.2:g.46010935G= GRCh38
NC_000020.10:g.44639574G= , CM000682.1:g.44639574G= GRCh37
NC_000020.9:g.44072981G= NCBI36
NG_011468.1:g.7028G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.534G= MANE Select ENSP00000361405.3:p.Gly178=
NM_004994.2:c.534G= NP_004985.2:p.Gly178=
NM_004994.3:c.534G= MANE Select NP_004985.2:p.Gly178=