Canonical Allele Identifier: CA510642494
Gene: MMP9 HGNC NCBI

Linked Data

gnomAD v4: 20-46011575-A-G
MyVariant Identifiers: chr20:g.44640214A>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011575A>G , CM000682.2:g.46011575A>G GRCh38
NC_000020.10:g.44640214A>G , CM000682.1:g.44640214A>G GRCh37
NC_000020.9:g.44073621A>G NCBI36
NG_011468.1:g.7668A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.825A>G MANE Select ENSP00000361405.3:p.Arg275=
NM_004994.2:c.825A>G NP_004985.2:p.Arg275=
NM_004994.3:c.825A>G MANE Select NP_004985.2:p.Arg275=
Search 100 bp 5'
Search 100 bp 3'