Canonical Allele Identifier: CA9886479

Gene: MMP9

Linked Data

• dbSNP Id: rs760872717
• ExAC: 20:44639775 C / T
• gnomAD v2: 20-44639775-C-T
• gnomAD v3: 20-46011136-C-T
• gnomAD v4: 20-46011136-C-T
• MyVariant Identifiers: chr20:g.44639775C>T (hg19) ; chr20:g.46011136C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46011136C>T , CM000682.2:g.46011136C>T	GRCh38
NC_000020.10:g.44639775C>T , CM000682.1:g.44639775C>T	GRCh37
NC_000020.9:g.44073182C>T	NCBI36
NG_011468.1:g.7229C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372330.3:c.650-7C>T MANE Select	ENSP00000361405.3:n.650-7C>T
NM_004994.2:c.650-7C>T	NP_004985.2:n.650-7C>T
NM_004994.3:c.650-7C>T MANE Select	NP_004985.2:n.650-7C>T