Canonical Allele Identifier: CA315639695
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs1056628

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46016407A>C , CM000682.2:g.46016407A>C GRCh38
NC_000020.10:g.44645046A>C , CM000682.1:g.44645046A>C GRCh37
NC_000020.9:g.44078453A>C NCBI36
NG_011468.1:g.12500A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000372330.3:c.*39A>C MANE Select ENSP00000361405.3:p.=
NM_004994.2:c.*39A>C NP_004985.2:p.=
NR_147699.1:n.669-1619T>G
NM_004994.3:c.*39A>C MANE Select NP_004985.2:p.=