Canonical Allele Identifier: CA9886431
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs775295226
ExAC: 20:44639567 G / A
gnomAD v2: 20-44639567-G-A
gnomAD v4: 20-46010928-G-A
MyVariant Identifiers: chr20:g.44639567G>A (hg19) chr20:g.46010928G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46010928G>A , CM000682.2:g.46010928G>A GRCh38
NC_000020.10:g.44639567G>A , CM000682.1:g.44639567G>A GRCh37
NC_000020.9:g.44072974G>A NCBI36
NG_011468.1:g.7021G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.527G>A MANE Select ENSP00000361405.3:p.Gly176Glu
NM_004994.2:c.527G>A NP_004985.2:p.Gly176Glu
NM_004994.3:c.527G>A MANE Select NP_004985.2:p.Gly176Glu
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