Canonical Allele Identifier: CA2653118062

Gene: MMP9

Linked Data

• gnomAD v4: 20-46011142-G-GTT

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46011143_46011144insTT , CM000682.2:g.46011143_46011144insTT	GRCh38
NC_000020.10:g.44639782_44639783insTT , CM000682.1:g.44639782_44639783insTT	GRCh37
NC_000020.9:g.44073189_44073190insTT	NCBI36
NG_011468.1:g.7236_7237insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372330.3:c.650_651insTT MANE Select	ENSP00000361405.3:p.Val218TrpfsTer?
NM_004994.2:c.650_651insTT	NP_004985.2:p.Val218TrpfsTer?
NM_004994.3:c.650_651insTT MANE Select	NP_004985.2:p.Val218TrpfsTer?