Canonical Allele Identifier: CA510642195
Gene: MMP9 HGNC NCBI

Linked Data

gnomAD v4: 20-46010063-C-A
MyVariant Identifiers: chr20:g.44638702C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46010063C>A , CM000682.2:g.46010063C>A GRCh38
NC_000020.10:g.44638702C>A , CM000682.1:g.44638702C>A GRCh37
NC_000020.9:g.44072109C>A NCBI36
NG_011468.1:g.6156C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000372330.3:c.336C>A MANE Select ENSP00000361405.3:p.Gly112=
NM_004994.2:c.336C>A NP_004985.2:p.Gly112=
NM_004994.3:c.336C>A MANE Select NP_004985.2:p.Gly112=
Search 100 bp 5'
Search 100 bp 3'