Canonical Allele Identifier: CA636176860
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs1361536607
gnomAD v2: 20-44640429-C-A
gnomAD v4: 20-46011790-C-A
MyVariant Identifiers: chr20:g.44640429C>A (hg19) chr20:g.46011790C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011790C>A , CM000682.2:g.46011790C>A GRCh38
NC_000020.10:g.44640429C>A , CM000682.1:g.44640429C>A GRCh37
NC_000020.9:g.44073836C>A NCBI36
NG_011468.1:g.7883C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.997+43C>A MANE Select ENSP00000361405.3:n.997+43C>A
NM_004994.2:c.997+43C>A NP_004985.2:n.997+43C>A
NM_004994.3:c.997+43C>A MANE Select NP_004985.2:n.997+43C>A
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