Canonical Allele Identifier: CA510642048
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs1412073569
gnomAD v2: 20-44638591-G-A
gnomAD v4: 20-46009952-G-A
MyVariant Identifiers: chr20:g.44638591G>A (hg19) chr20:g.46009952G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46009952G>A , CM000682.2:g.46009952G>A GRCh38
NC_000020.10:g.44638591G>A , CM000682.1:g.44638591G>A GRCh37
NC_000020.9:g.44071998G>A NCBI36
NG_011468.1:g.6045G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000372330.3:c.225G>A MANE Select ENSP00000361405.3:p.Gln75=
NM_004994.2:c.225G>A NP_004985.2:p.Gln75=
NM_004994.3:c.225G>A MANE Select NP_004985.2:p.Gln75=
Search 100 bp 5'
Search 100 bp 3'