Canonical Allele Identifier: CA409213739
Gene: MMP9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2920385
ClinVar RCV Id: RCV003736267
MyVariant Identifiers: chr20:g.44639896G>A (hg19) chr20:g.46011257G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011257G>A , CM000682.2:g.46011257G>A GRCh38
NC_000020.10:g.44639896G>A , CM000682.1:g.44639896G>A GRCh37
NC_000020.9:g.44073303G>A NCBI36
NG_011468.1:g.7350G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.764G>A MANE Select ENSP00000361405.3:p.Trp255Ter
NM_004994.2:c.764G>A NP_004985.2:p.Trp255Ter
NM_004994.3:c.764G>A MANE Select NP_004985.2:p.Trp255Ter
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