Canonical Allele Identifier: CA636176591

Gene: MMP9

Linked Data

• dbSNP Id: rs1266487132
• gnomAD v2: 20-44639693-A-T
• gnomAD v3: 20-46011054-A-T
• gnomAD v4: 20-46011054-A-T
• MyVariant Identifiers: chr20:g.44639693A>T (hg19) ; chr20:g.46011054A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46011054A>T , CM000682.2:g.46011054A>T	GRCh38
NC_000020.10:g.44639693A>T , CM000682.1:g.44639693A>T	GRCh37
NC_000020.9:g.44073100A>T	NCBI36
NG_011468.1:g.7147A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372330.3:c.649+4A>T MANE Select	ENSP00000361405.3:n.649+4A>T
NM_004994.2:c.649+4A>T	NP_004985.2:n.649+4A>T
NM_004994.3:c.649+4A>T MANE Select	NP_004985.2:n.649+4A>T