Canonical Allele Identifier: CA9886461
Gene: MMP9 HGNC NCBI

Linked Data

ClinVar Variation Id: 338548
dbSNP Id: rs2274755

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011053G>T , CM000682.2:g.46011053G>T GRCh38
NC_000020.10:g.44639692G>T , CM000682.1:g.44639692G>T GRCh37
NC_000020.9:g.44073099G>T NCBI36
NG_011468.1:g.7146G>T

Transcript Alleles

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