Canonical Allele Identifier: CA1017939871
Gene: MMP9 HGNC NCBI
SLC12A5-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2084323750
gnomAD v3: 20-46016523-T-C
gnomAD v4: 20-46016523-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46016523T>C , CM000682.2:g.46016523T>C GRCh38
NC_000020.10:g.44645162T>C , CM000682.1:g.44645162T>C GRCh37
NC_000020.9:g.44078569T>C NCBI36
NG_011468.1:g.12616T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000372330.3:c.*155T>C (MMP9) MANE Select ENSP00000361405.3:n.*155T>C
NM_004994.2:c.*155T>C (MMP9) NP_004985.2:n.*155T>C
NR_147699.1:n.669-1735A>G (SLC12A5-AS1)
NM_004994.3:c.*155T>C (MMP9) MANE Select NP_004985.2:n.*155T>C
Search 100 bp 5'
Search 100 bp 3'