Canonical Allele Identifier: CA409212912
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs55789927

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46010960C>A , CM000682.2:g.46010960C>A GRCh38
NC_000020.10:g.44639599C>A , CM000682.1:g.44639599C>A GRCh37
NC_000020.9:g.44073006C>A NCBI36
NG_011468.1:g.7053C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000372330.3:c.559C>A MANE Select ENSP00000361405.3:p.Leu187Ile
NM_004994.2:c.559C>A NP_004985.2:p.Leu187Ile
NM_004994.3:c.559C>A MANE Select NP_004985.2:p.Leu187Ile