Canonical Allele Identifier: CA2366478223
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs79845319
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46010332A>T , CM000682.2:g.46010332A>T GRCh38
NC_000020.10:g.44638971A>T , CM000682.1:g.44638971A>T GRCh37
NC_000020.9:g.44072378A>T NCBI36
NG_011468.1:g.6425A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000372330.3:c.372-151A>T MANE Select ENSP00000361405.3:n.372-151A>T
NM_004994.2:c.372-151A>T NP_004985.2:n.372-151A>T
NM_004994.3:c.372-151A>T MANE Select NP_004985.2:n.372-151A>T
Search 100 bp 5'
Search 100 bp 3'