Canonical Allele Identifier: CA2366478492
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs2084273877
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46010836C>G , CM000682.2:g.46010836C>G GRCh38
NC_000020.10:g.44639475C>G , CM000682.1:g.44639475C>G GRCh37
NC_000020.9:g.44072882C>G NCBI36
NG_011468.1:g.6929C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.521-86C>G MANE Select ENSP00000361405.3:n.521-86C>G
NM_004994.2:c.521-86C>G NP_004985.2:n.521-86C>G
NM_004994.3:c.521-86C>G MANE Select NP_004985.2:n.521-86C>G
Search 100 bp 5'
Search 100 bp 3'