Canonical Allele Identifier: CA409227732
Gene: MMP9 HGNC NCBI
SLC12A5-AS1 HGNC NCBI

Linked Data

gnomAD v4: 20-46016300-A-C
MyVariant Identifiers: chr20:g.44644939A>C (hg19) chr20:g.46016300A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46016300A>C , CM000682.2:g.46016300A>C GRCh38
NC_000020.10:g.44644939A>C , CM000682.1:g.44644939A>C GRCh37
NC_000020.9:g.44078346A>C NCBI36
NG_011468.1:g.12393A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.2056A>C (MMP9) MANE Select ENSP00000361405.3:p.Ser686Arg
NM_004994.2:c.2056A>C (MMP9) NP_004985.2:p.Ser686Arg
NR_147699.1:n.669-1512T>G (SLC12A5-AS1)
NM_004994.3:c.2056A>C (MMP9) MANE Select NP_004985.2:p.Ser686Arg
Search 100 bp 5'
Search 100 bp 3'