Canonical Allele Identifier: CA409212904
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs1804032623

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46010955A>G , CM000682.2:g.46010955A>G GRCh38
NC_000020.10:g.44639594A>G , CM000682.1:g.44639594A>G GRCh37
NC_000020.9:g.44073001A>G NCBI36
NG_011468.1:g.7048A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.554A>G MANE Select ENSP00000361405.3:p.Asp185Gly
NM_004994.2:c.554A>G NP_004985.2:p.Asp185Gly
NM_004994.3:c.554A>G MANE Select NP_004985.2:p.Asp185Gly