Canonical Allele Identifier: CA9886433
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs768898768
ExAC: 20:44639576 A / G
gnomAD v2: 20-44639576-A-G
gnomAD v3: 20-46010937-A-G
gnomAD v4: 20-46010937-A-G
MyVariant Identifiers: chr20:g.44639576A>G (hg19) chr20:g.46010937A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46010937A>G , CM000682.2:g.46010937A>G GRCh38
NC_000020.10:g.44639576A>G , CM000682.1:g.44639576A>G GRCh37
NC_000020.9:g.44072983A>G NCBI36
NG_011468.1:g.7030A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.536A>G MANE Select ENSP00000361405.3:p.Tyr179Cys
NM_004994.2:c.536A>G NP_004985.2:p.Tyr179Cys
NM_004994.3:c.536A>G MANE Select NP_004985.2:p.Tyr179Cys
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