Canonical Allele Identifier: CA409211918

Gene: MMP9

Linked Data

• dbSNP Id: rs2084264553
• gnomAD v3: 20-46009962-T-G
• gnomAD v4: 20-46009962-T-G
• MyVariant Identifiers: chr20:g.44638601T>G (hg19) ; chr20:g.46009962T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46009962T>G , CM000682.2:g.46009962T>G	GRCh38
NC_000020.10:g.44638601T>G , CM000682.1:g.44638601T>G	GRCh37
NC_000020.9:g.44072008T>G	NCBI36
NG_011468.1:g.6055T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372330.3:c.235T>G MANE Select	ENSP00000361405.3:p.Ser79Ala
NM_004994.2:c.235T>G	NP_004985.2:p.Ser79Ala
NM_004994.3:c.235T>G MANE Select	NP_004985.2:p.Ser79Ala