Canonical Allele Identifier: CA409215467
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs371340871

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011711G>A , CM000682.2:g.46011711G>A GRCh38
NC_000020.10:g.44640350G>A , CM000682.1:g.44640350G>A GRCh37
NC_000020.9:g.44073757G>A NCBI36
NG_011468.1:g.7804G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.961G>A MANE Select ENSP00000361405.3:p.Asp321Asn
NM_004994.2:c.961G>A NP_004985.2:p.Asp321Asn
NM_004994.3:c.961G>A MANE Select NP_004985.2:p.Asp321Asn