Canonical Allele Identifier: CA510751655
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs2084274736
gnomAD v4: 20-46010959-G-A
MyVariant Identifiers: chr20:g.44639598G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46010959G>A , CM000682.2:g.46010959G>A GRCh38
NC_000020.10:g.44639598G>A , CM000682.1:g.44639598G>A GRCh37
NC_000020.9:g.44073005G>A NCBI36
NG_011468.1:g.7052G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.558G>A MANE Select ENSP00000361405.3:p.Gly186=
NM_004994.2:c.558G>A NP_004985.2:p.Gly186=
NM_004994.3:c.558G>A MANE Select NP_004985.2:p.Gly186=
Search 100 bp 5'
Search 100 bp 3'