Canonical Allele Identifier: CA636176597
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs1448241384
gnomAD v2: 20-44639745-C-T
gnomAD v3: 20-46011106-C-T
gnomAD v4: 20-46011106-C-T
MyVariant Identifiers: chr20:g.44639745C>T (hg19) chr20:g.46011106C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011106C>T , CM000682.2:g.46011106C>T GRCh38
NC_000020.10:g.44639745C>T , CM000682.1:g.44639745C>T GRCh37
NC_000020.9:g.44073152C>T NCBI36
NG_011468.1:g.7199C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.650-37C>T MANE Select ENSP00000361405.3:n.650-37C>T
NM_004994.2:c.650-37C>T NP_004985.2:n.650-37C>T
NM_004994.3:c.650-37C>T MANE Select NP_004985.2:n.650-37C>T
Search 100 bp 5'
Search 100 bp 3'