Canonical Allele Identifier: CA636176586

Gene: MMP9

Linked Data

• dbSNP Id: rs1360816192
• gnomAD v2: 20-44639988-GC-G
• gnomAD v4: 20-46011349-GC-G
• MyVariant Identifiers: chr20:g.44639989del (hg19) ; chr20:g.46011350del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46011352del , CM000682.2:g.46011352del	GRCh38
NC_000020.10:g.44639991del , CM000682.1:g.44639991del	GRCh37
NC_000020.9:g.44073398del	NCBI36
NG_011468.1:g.7445del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372330.3:c.823+36del MANE Select	ENSP00000361405.3:n.823+36del
NM_004994.2:c.823+36del	NP_004985.2:n.823+36del
NM_004994.3:c.823+36del MANE Select	NP_004985.2:n.823+36del