Canonical Allele Identifier: CA409211932

Gene: MMP9

Linked Data

• MyVariant Identifiers: chr20:g.44638607C>G (hg19) ; chr20:g.46009968C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46009968C>G , CM000682.2:g.46009968C>G	GRCh38
NC_000020.10:g.44638607C>G , CM000682.1:g.44638607C>G	GRCh37
NC_000020.9:g.44072014C>G	NCBI36
NG_011468.1:g.6061C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372330.3:c.241C>G MANE Select	ENSP00000361405.3:p.Pro81Ala
NM_004994.2:c.241C>G	NP_004985.2:p.Pro81Ala
NM_004994.3:c.241C>G MANE Select	NP_004985.2:p.Pro81Ala