Canonical Allele Identifier: CA1017937680
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs2084266692
gnomAD v3: 20-46010170-A-G
gnomAD v4: 20-46010170-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46010170A>G , CM000682.2:g.46010170A>G GRCh38
NC_000020.10:g.44638809A>G , CM000682.1:g.44638809A>G GRCh37
NC_000020.9:g.44072216A>G NCBI36
NG_011468.1:g.6263A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.371+72A>G MANE Select ENSP00000361405.3:n.371+72A>G
NM_004994.2:c.371+72A>G NP_004985.2:n.371+72A>G
NM_004994.3:c.371+72A>G MANE Select NP_004985.2:n.371+72A>G
Search 100 bp 5'
Search 100 bp 3'