Canonical Allele Identifier: CA636176589
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs1267991562
gnomAD v2: 20-44640057-A-AC
gnomAD v3: 20-46011418-A-AC
gnomAD v4: 20-46011418-A-AC
MyVariant Identifiers: chr20:g.44640057_44640058insC (hg19) chr20:g.46011418_46011419insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011421dup , CM000682.2:g.46011421dup GRCh38
NC_000020.10:g.44640060dup , CM000682.1:g.44640060dup GRCh37
NC_000020.9:g.44073467dup NCBI36
NG_011468.1:g.7514dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.823+105dup MANE Select ENSP00000361405.3:n.823+105dup
NM_004994.2:c.823+105dup NP_004985.2:n.823+105dup
NM_004994.3:c.823+105dup MANE Select NP_004985.2:n.823+105dup
Search 100 bp 5'
Search 100 bp 3'