Canonical Allele Identifier: CA920222505
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs1568847615

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011788_46011789del , CM000682.2:g.46011788_46011789del GRCh38
NC_000020.10:g.44640427_44640428del , CM000682.1:g.44640427_44640428del GRCh37
NC_000020.9:g.44073834_44073835del NCBI36
NG_011468.1:g.7881_7882del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.997+41_997+42del MANE Select ENSP00000361405.3:n.997+41_997+42del
NM_004994.2:c.997+41_997+42del NP_004985.2:n.997+41_997+42del
NM_004994.3:c.997+41_997+42del MANE Select NP_004985.2:n.997+41_997+42del