Canonical Allele Identifier: CA510751678
Gene: MMP9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.44639616T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46010977T>C , CM000682.2:g.46010977T>C GRCh38
NC_000020.10:g.44639616T>C , CM000682.1:g.44639616T>C GRCh37
NC_000020.9:g.44073023T>C NCBI36
NG_011468.1:g.7070T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.576T>C MANE Select ENSP00000361405.3:p.Phe192=
NM_004994.2:c.576T>C NP_004985.2:p.Phe192=
NM_004994.3:c.576T>C MANE Select NP_004985.2:p.Phe192=
Search 100 bp 5'
Search 100 bp 3'