Canonical Allele Identifier: CA409215660
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs1195542011
gnomAD v4: 20-46011749-T-G
MyVariant Identifiers: chr20:g.44640388T>G (hg19) chr20:g.46011749T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011749T>G , CM000682.2:g.46011749T>G GRCh38
NC_000020.10:g.44640388T>G , CM000682.1:g.44640388T>G GRCh37
NC_000020.9:g.44073795T>G NCBI36
NG_011468.1:g.7842T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.997+2T>G MANE Select ENSP00000361405.3:n.997+2T>G
NM_004994.2:c.997+2T>G NP_004985.2:n.997+2T>G
NM_004994.3:c.997+2T>G MANE Select NP_004985.2:n.997+2T>G
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Search 100 bp 3'