Canonical Allele Identifier: CA315634717

Gene: MMP9

Linked Data

• dbSNP Id: rs754620582
• gnomAD v2: 20-44639474-A-G
• gnomAD v3: 20-46010835-A-G
• gnomAD v4: 20-46010835-A-G
• MyVariant Identifiers: chr20:g.44639474A>G (hg19) ; chr20:g.46010835A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46010835A>G , CM000682.2:g.46010835A>G	GRCh38
NC_000020.10:g.44639474A>G , CM000682.1:g.44639474A>G	GRCh37
NC_000020.9:g.44072881A>G	NCBI36
NG_011468.1:g.6928A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372330.3:c.521-87A>G MANE Select	ENSP00000361405.3:n.521-87A>G
NM_004994.2:c.521-87A>G	NP_004985.2:n.521-87A>G
NM_004994.3:c.521-87A>G MANE Select	NP_004985.2:n.521-87A>G