Canonical Allele Identifier: CA409214565

Gene: MMP9

Linked Data

• MyVariant Identifiers: chr20:g.44640233A>C (hg19) ; chr20:g.46011594A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46011594A>C , CM000682.2:g.46011594A>C	GRCh38
NC_000020.10:g.44640233A>C , CM000682.1:g.44640233A>C	GRCh37
NC_000020.9:g.44073640A>C	NCBI36
NG_011468.1:g.7687A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000372330.3:c.844A>C MANE Select	ENSP00000361405.3:p.Asn282His
NM_004994.2:c.844A>C	NP_004985.2:p.Asn282His
NM_004994.3:c.844A>C MANE Select	NP_004985.2:p.Asn282His