Canonical Allele Identifier: CA315634967
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs201667517

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011075C>T , CM000682.2:g.46011075C>T GRCh38
NC_000020.10:g.44639714C>T , CM000682.1:g.44639714C>T GRCh37
NC_000020.9:g.44073121C>T NCBI36
NG_011468.1:g.7168C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000372330.3:c.649+25C>T MANE Select ENSP00000361405.3:n.649+25C>T
NM_004994.2:c.649+25C>T NP_004985.2:n.649+25C>T
NM_004994.3:c.649+25C>T MANE Select NP_004985.2:n.649+25C>T