Canonical Allele Identifier: CA2653118619
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs1193340319
gnomAD v4: 20-46011492-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011492G>A , CM000682.2:g.46011492G>A GRCh38
NC_000020.10:g.44640131G>A , CM000682.1:g.44640131G>A GRCh37
NC_000020.9:g.44073538G>A NCBI36
NG_011468.1:g.7585G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000372330.3:c.824-82G>A MANE Select ENSP00000361405.3:n.824-82G>A
NM_004994.2:c.824-82G>A NP_004985.2:n.824-82G>A
NM_004994.3:c.824-82G>A MANE Select NP_004985.2:n.824-82G>A
Search 100 bp 5'
Search 100 bp 3'