Canonical Allele Identifier: CA409212999
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs1187196678
gnomAD v3: 20-46011004-C-G
gnomAD v4: 20-46011004-C-G
MyVariant Identifiers: chr20:g.44639643C>G (hg19) chr20:g.46011004C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011004C>G , CM000682.2:g.46011004C>G GRCh38
NC_000020.10:g.44639643C>G , CM000682.1:g.44639643C>G GRCh37
NC_000020.9:g.44073050C>G NCBI36
NG_011468.1:g.7097C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.603C>G MANE Select ENSP00000361405.3:p.Asp201Glu
NM_004994.2:c.603C>G NP_004985.2:p.Asp201Glu
NM_004994.3:c.603C>G MANE Select NP_004985.2:p.Asp201Glu
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