Canonical Allele Identifier: CA9886531
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs756898923
ExAC: 20:44640170 T / G
gnomAD v2: 20-44640170-T-G
gnomAD v3: 20-46011531-T-G
gnomAD v4: 20-46011531-T-G
MyVariant Identifiers: chr20:g.44640170T>G (hg19) chr20:g.46011531T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011531T>G , CM000682.2:g.46011531T>G GRCh38
NC_000020.10:g.44640170T>G , CM000682.1:g.44640170T>G GRCh37
NC_000020.9:g.44073577T>G NCBI36
NG_011468.1:g.7624T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.824-43T>G MANE Select ENSP00000361405.3:n.824-43T>G
NM_004994.2:c.824-43T>G NP_004985.2:n.824-43T>G
NM_004994.3:c.824-43T>G MANE Select NP_004985.2:n.824-43T>G
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