Canonical Allele Identifier: CA9886533
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs750775134
ExAC: 20:44640172 T / C
gnomAD v2: 20-44640172-T-C
gnomAD v4: 20-46011533-T-C
COSMIC: COSN20065999
MyVariant Identifiers: chr20:g.44640172T>C (hg19) chr20:g.46011533T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011533T>C , CM000682.2:g.46011533T>C GRCh38
NC_000020.10:g.44640172T>C , CM000682.1:g.44640172T>C GRCh37
NC_000020.9:g.44073579T>C NCBI36
NG_011468.1:g.7626T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.824-41T>C MANE Select ENSP00000361405.3:n.824-41T>C
NM_004994.2:c.824-41T>C NP_004985.2:n.824-41T>C
NM_004994.3:c.824-41T>C MANE Select NP_004985.2:n.824-41T>C
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