Canonical Allele Identifier: CA9886439
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs763027034

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46010956C>T , CM000682.2:g.46010956C>T GRCh38
NC_000020.10:g.44639595C>T , CM000682.1:g.44639595C>T GRCh37
NC_000020.9:g.44073002C>T NCBI36
NG_011468.1:g.7049C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000372330.3:c.555C>T MANE Select ENSP00000361405.3:p.Asp185=
NM_004994.2:c.555C>T NP_004985.2:p.Asp185=
NM_004994.3:c.555C>T MANE Select NP_004985.2:p.Asp185=