Canonical Allele Identifier: CA744849014
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs1458686782

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011510C>T , CM000682.2:g.46011510C>T GRCh38
NC_000020.10:g.44640149C>T , CM000682.1:g.44640149C>T GRCh37
NC_000020.9:g.44073556C>T NCBI36
NG_011468.1:g.7603C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000372330.3:c.824-64C>T MANE Select ENSP00000361405.3:n.824-64C>T
NM_004994.2:c.824-64C>T NP_004985.2:n.824-64C>T
NM_004994.3:c.824-64C>T MANE Select NP_004985.2:n.824-64C>T