Canonical Allele Identifier: CA9886909
Gene: MMP9 HGNC NCBI
SLC12A5-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs759118773
ExAC: 20:44645044 C / T
gnomAD v2: 20-44645044-C-T
gnomAD v3: 20-46016405-C-T
gnomAD v4: 20-46016405-C-T
MyVariant Identifiers: chr20:g.44645044C>T (hg19) chr20:g.46016405C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46016405C>T , CM000682.2:g.46016405C>T GRCh38
NC_000020.10:g.44645044C>T , CM000682.1:g.44645044C>T GRCh37
NC_000020.9:g.44078451C>T NCBI36
NG_011468.1:g.12498C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.*37C>T (MMP9) MANE Select ENSP00000361405.3:n.*37C>T
NM_004994.2:c.*37C>T (MMP9) NP_004985.2:n.*37C>T
NR_147699.1:n.669-1617G>A (SLC12A5-AS1)
NM_004994.3:c.*37C>T (MMP9) MANE Select NP_004985.2:n.*37C>T
Search 100 bp 5'
Search 100 bp 3'