Canonical Allele Identifier: CA409214440
Gene: MMP9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011582A>T , CM000682.2:g.46011582A>T GRCh38
NC_000020.10:g.44640221A>T , CM000682.1:g.44640221A>T GRCh37
NC_000020.9:g.44073628A>T NCBI36
NG_011468.1:g.7675A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.832A>T MANE Select ENSP00000361405.3:p.Thr278Ser
NM_004994.2:c.832A>T NP_004985.2:p.Thr278Ser
NM_004994.3:c.832A>T MANE Select NP_004985.2:p.Thr278Ser