Canonical Allele Identifier: CA744849008
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs1231990633
gnomAD v4: 20-46011499-A-C
MyVariant Identifiers: chr20:g.44640138A>C (hg19) chr20:g.46011499A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011499A>C , CM000682.2:g.46011499A>C GRCh38
NC_000020.10:g.44640138A>C , CM000682.1:g.44640138A>C GRCh37
NC_000020.9:g.44073545A>C NCBI36
NG_011468.1:g.7592A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000372330.3:c.824-75A>C MANE Select ENSP00000361405.3:n.824-75A>C
NM_004994.2:c.824-75A>C NP_004985.2:n.824-75A>C
NM_004994.3:c.824-75A>C MANE Select NP_004985.2:n.824-75A>C
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