Canonical Allele Identifier: CA2366481123
Gene: MMP9 HGNC NCBI
SLC12A5-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46016437T= , CM000682.2:g.46016437T= GRCh38
NC_000020.10:g.44645076T= , CM000682.1:g.44645076T= GRCh37
NC_000020.9:g.44078483T= NCBI36
NG_011468.1:g.12530T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.*69T= (MMP9) MANE Select ENSP00000361405.3:n.*69T=
NM_004994.2:c.*69T= (MMP9) NP_004985.2:n.*69T=
NR_147699.1:n.669-1649A= (SLC12A5-AS1)
NM_004994.3:c.*69T= (MMP9) MANE Select NP_004985.2:n.*69T=