Canonical Allele Identifier: CA9886466
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs201895856

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011098A>G , CM000682.2:g.46011098A>G GRCh38
NC_000020.10:g.44639737A>G , CM000682.1:g.44639737A>G GRCh37
NC_000020.9:g.44073144A>G NCBI36
NG_011468.1:g.7191A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000372330.3:c.650-45A>G MANE Select ENSP00000361405.3:n.650-45A>G
NM_004994.2:c.650-45A>G NP_004985.2:n.650-45A>G
NM_004994.3:c.650-45A>G MANE Select NP_004985.2:n.650-45A>G