Canonical Allele Identifier: CA2366481077
Gene: MMP9 HGNC NCBI
SLC12A5-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46016303G= , CM000682.2:g.46016303G= GRCh38
NC_000020.10:g.44644942G= , CM000682.1:g.44644942G= GRCh37
NC_000020.9:g.44078349G= NCBI36
NG_011468.1:g.12396G=

Transcript Alleles

HGVS Amino-acid change
ENST00000372330.3:c.2059G= (MMP9) MANE Select ENSP00000361405.3:p.Glu687=
NM_004994.2:c.2059G= (MMP9) NP_004985.2:p.Glu687=
NR_147699.1:n.669-1515C= (SLC12A5-AS1)
NM_004994.3:c.2059G= (MMP9) MANE Select NP_004985.2:p.Glu687=