Canonical Allele Identifier: CA409213377

Gene: MMP9

Linked Data

• COSMIC: COSM4794244
• MyVariant Identifiers: chr20:g.44639829C>T (hg19) ; chr20:g.46011190C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46011190C>T , CM000682.2:g.46011190C>T	GRCh38
NC_000020.10:g.44639829C>T , CM000682.1:g.44639829C>T	GRCh37
NC_000020.9:g.44073236C>T	NCBI36
NG_011468.1:g.7283C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372330.3:c.697C>T MANE Select	ENSP00000361405.3:p.Pro233Ser
NM_004994.2:c.697C>T	NP_004985.2:p.Pro233Ser
NM_004994.3:c.697C>T MANE Select	NP_004985.2:p.Pro233Ser