Canonical Allele Identifier: CA2366478542
Gene: MMP9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46010942T= , CM000682.2:g.46010942T= GRCh38
NC_000020.10:g.44639581T= , CM000682.1:g.44639581T= GRCh37
NC_000020.9:g.44072988T= NCBI36
NG_011468.1:g.7035T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.541T= MANE Select ENSP00000361405.3:p.Phe181=
NM_004994.2:c.541T= NP_004985.2:p.Phe181=
NM_004994.3:c.541T= MANE Select NP_004985.2:p.Phe181=
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