Canonical Allele Identifier: CA636176594
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs1198427745
gnomAD v2: 20-44639716-T-A
gnomAD v4: 20-46011077-T-A
MyVariant Identifiers: chr20:g.44639716T>A (hg19) chr20:g.46011077T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011077T>A , CM000682.2:g.46011077T>A GRCh38
NC_000020.10:g.44639716T>A , CM000682.1:g.44639716T>A GRCh37
NC_000020.9:g.44073123T>A NCBI36
NG_011468.1:g.7170T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000372330.3:c.649+27T>A MANE Select ENSP00000361405.3:n.649+27T>A
NM_004994.2:c.649+27T>A NP_004985.2:n.649+27T>A
NM_004994.3:c.649+27T>A MANE Select NP_004985.2:n.649+27T>A
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