Canonical Allele Identifier: CA2366478979
Gene: MMP9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011795A= , CM000682.2:g.46011795A= GRCh38
NC_000020.10:g.44640434A= , CM000682.1:g.44640434A= GRCh37
NC_000020.9:g.44073841A= NCBI36
NG_011468.1:g.7888A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.997+48A= MANE Select ENSP00000361405.3:n.997+48A=
NM_004994.2:c.997+48A= NP_004985.2:n.997+48A=
NM_004994.3:c.997+48A= MANE Select NP_004985.2:n.997+48A=
Search 100 bp 5'
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