Canonical Allele Identifier: CA409213379

Gene: MMP9

Linked Data

• dbSNP Id: rs1302811072
• gnomAD v2: 20-44639830-C-G
• MyVariant Identifiers: chr20:g.44639830C>G (hg19) ; chr20:g.46011191C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46011191C>G , CM000682.2:g.46011191C>G	GRCh38
NC_000020.10:g.44639830C>G , CM000682.1:g.44639830C>G	GRCh37
NC_000020.9:g.44073237C>G	NCBI36
NG_011468.1:g.7284C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372330.3:c.698C>G MANE Select	ENSP00000361405.3:p.Pro233Arg
NM_004994.2:c.698C>G	NP_004985.2:p.Pro233Arg
NM_004994.3:c.698C>G MANE Select	NP_004985.2:p.Pro233Arg