Canonical Allele Identifier: CA2366481066
Gene: MMP9 HGNC NCBI
SLC12A5-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46016285C= , CM000682.2:g.46016285C= GRCh38
NC_000020.10:g.44644924C= , CM000682.1:g.44644924C= GRCh37
NC_000020.9:g.44078331C= NCBI36
NG_011468.1:g.12378C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.2041C= (MMP9) MANE Select ENSP00000361405.3:p.Arg681=
NM_004994.2:c.2041C= (MMP9) NP_004985.2:p.Arg681=
NR_147699.1:n.669-1497G= (SLC12A5-AS1)
NM_004994.3:c.2041C= (MMP9) MANE Select NP_004985.2:p.Arg681=
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