Canonical Allele Identifier: CA315639720
Gene: MMP9 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2664517

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46016464C>T , CM000682.2:g.46016464C>T GRCh38
NC_000020.10:g.44645103C>T , CM000682.1:g.44645103C>T GRCh37
NC_000020.9:g.44078510C>T NCBI36
NG_011468.1:g.12557C>T

Transcript Alleles

HGVS Amino-acid change
NM_004994.2:c.*96C>T VV NP_004985.2:p.=
NR_147699.1:n.669-1676G>A
NM_004994.3:c.*96C>T VV MANE Preferred NP_004985.2:p.=
ENST00000372330.3:c.*96C>T ENSP00000361405.3:p.=