Canonical Allele Identifier: CA2841770008
Gene: MMP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011532G>T , CM000682.2:g.46011532G>T GRCh38
NC_000020.10:g.44640171G>T , CM000682.1:g.44640171G>T GRCh37
NC_000020.9:g.44073578G>T NCBI36
NG_011468.1:g.7625G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.824-42G>T MANE Select ENSP00000361405.3:n.824-42G>T
NM_004994.2:c.824-42G>T NP_004985.2:n.824-42G>T
NM_004994.3:c.824-42G>T MANE Select NP_004985.2:n.824-42G>T