Canonical Allele Identifier: CA9886430
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs771781780
ExAC: 20:44639566 G / A
gnomAD v2: 20-44639566-G-A
gnomAD v4: 20-46010927-G-A
MyVariant Identifiers: chr20:g.44639566G>A (hg19) chr20:g.46010927G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46010927G>A , CM000682.2:g.46010927G>A GRCh38
NC_000020.10:g.44639566G>A , CM000682.1:g.44639566G>A GRCh37
NC_000020.9:g.44072973G>A NCBI36
NG_011468.1:g.7020G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.526G>A MANE Select ENSP00000361405.3:p.Gly176Arg
NM_004994.2:c.526G>A NP_004985.2:p.Gly176Arg
NM_004994.3:c.526G>A MANE Select NP_004985.2:p.Gly176Arg
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