Canonical Allele Identifier: CA2577206036
Gene: MMP9 HGNC NCBI

Linked Data

gnomAD v4: 20-46011788-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011788A>C , CM000682.2:g.46011788A>C GRCh38
NC_000020.10:g.44640427A>C , CM000682.1:g.44640427A>C GRCh37
NC_000020.9:g.44073834A>C NCBI36
NG_011468.1:g.7881A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.997+41A>C MANE Select ENSP00000361405.3:n.997+41A>C
NM_004994.2:c.997+41A>C NP_004985.2:n.997+41A>C
NM_004994.3:c.997+41A>C MANE Select NP_004985.2:n.997+41A>C
Search 100 bp 5'
Search 100 bp 3'