Canonical Allele Identifier: CA636039131
Gene: MMP9 HGNC NCBI
SLC12A5-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1362694625
gnomAD v2: 20-44644870-G-A
gnomAD v4: 20-46016231-G-A
MyVariant Identifiers: chr20:g.44644870G>A (hg19) chr20:g.46016231G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46016231G>A , CM000682.2:g.46016231G>A GRCh38
NC_000020.10:g.44644870G>A , CM000682.1:g.44644870G>A GRCh37
NC_000020.9:g.44078277G>A NCBI36
NG_011468.1:g.12324G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.2006-19G>A (MMP9) MANE Select ENSP00000361405.3:n.2006-19G>A
NM_004994.2:c.2006-19G>A (MMP9) NP_004985.2:n.2006-19G>A
NR_147699.1:n.669-1443C>T (SLC12A5-AS1)
NM_004994.3:c.2006-19G>A (MMP9) MANE Select NP_004985.2:n.2006-19G>A
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