Canonical Allele Identifier: CA409227636
Gene: MMP9 HGNC NCBI
SLC12A5-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2782800
ClinVar RCV Id: RCV003664199
dbSNP Id: rs1369630811

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46016292G>C , CM000682.2:g.46016292G>C GRCh38
NC_000020.10:g.44644931G>C , CM000682.1:g.44644931G>C GRCh37
NC_000020.9:g.44078338G>C NCBI36
NG_011468.1:g.12385G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.2048G>C (MMP9) MANE Select ENSP00000361405.3:p.Ser683Thr
NM_004994.2:c.2048G>C (MMP9) NP_004985.2:p.Ser683Thr
NR_147699.1:n.669-1504C>G (SLC12A5-AS1)
NM_004994.3:c.2048G>C (MMP9) MANE Select NP_004985.2:p.Ser683Thr