Canonical Allele Identifier: CA315639743
Gene: MMP9 HGNC NCBI
SLC12A5-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs200642502

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46016547A>T , CM000682.2:g.46016547A>T GRCh38
NC_000020.10:g.44645186A>T , CM000682.1:g.44645186A>T GRCh37
NC_000020.9:g.44078593A>T NCBI36
NG_011468.1:g.12640A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.*179A>T (MMP9) MANE Select ENSP00000361405.3:n.*179A>T
NM_004994.2:c.*179A>T (MMP9) NP_004985.2:n.*179A>T
NR_147699.1:n.669-1759T>A (SLC12A5-AS1)
NM_004994.3:c.*179A>T (MMP9) MANE Select NP_004985.2:n.*179A>T