Canonical Allele Identifier: CA636176765

Gene: MMP9

Linked Data

• dbSNP Id: rs1318876673
• gnomAD v2: 20-44639519-C-A
• gnomAD v4: 20-46010880-C-A
• MyVariant Identifiers: chr20:g.44639519C>A (hg19) ; chr20:g.46010880C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46010880C>A , CM000682.2:g.46010880C>A	GRCh38
NC_000020.10:g.44639519C>A , CM000682.1:g.44639519C>A	GRCh37
NC_000020.9:g.44072926C>A	NCBI36
NG_011468.1:g.6973C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372330.3:c.521-42C>A MANE Select	ENSP00000361405.3:n.521-42C>A
NM_004994.2:c.521-42C>A	NP_004985.2:n.521-42C>A
NM_004994.3:c.521-42C>A MANE Select	NP_004985.2:n.521-42C>A