Canonical Allele Identifier: CA409213180
Gene: MMP9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011143T>C , CM000682.2:g.46011143T>C GRCh38
NC_000020.10:g.44639782T>C , CM000682.1:g.44639782T>C GRCh37
NC_000020.9:g.44073189T>C NCBI36
NG_011468.1:g.7236T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.650T>C MANE Select ENSP00000361405.3:p.Val217Ala
NM_004994.2:c.650T>C NP_004985.2:p.Val217Ala
NM_004994.3:c.650T>C MANE Select NP_004985.2:p.Val217Ala