Canonical Allele Identifier: CA9886529
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs761034760
ExAC: 20:44640164 ATG / A
gnomAD v2: 20-44640164-ATG-A
gnomAD v4: 20-46011525-ATG-A
MyVariant Identifiers: chr20:g.44640165_44640166del (hg19) chr20:g.46011526_46011527del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011528_46011529del , CM000682.2:g.46011528_46011529del GRCh38
NC_000020.10:g.44640167_44640168del , CM000682.1:g.44640167_44640168del GRCh37
NC_000020.9:g.44073574_44073575del NCBI36
NG_011468.1:g.7621_7622del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.824-46_824-45del MANE Select ENSP00000361405.3:n.824-46_824-45del
NM_004994.2:c.824-46_824-45del NP_004985.2:n.824-46_824-45del
NM_004994.3:c.824-46_824-45del MANE Select NP_004985.2:n.824-46_824-45del
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