Canonical Allele Identifier: CA409213741

Gene: MMP9

Linked Data

• gnomAD v4: 20-46011257-G-C
• MyVariant Identifiers: chr20:g.44639896G>C (hg19) ; chr20:g.46011257G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46011257G>C , CM000682.2:g.46011257G>C	GRCh38
NC_000020.10:g.44639896G>C , CM000682.1:g.44639896G>C	GRCh37
NC_000020.9:g.44073303G>C	NCBI36
NG_011468.1:g.7350G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372330.3:c.764G>C MANE Select	ENSP00000361405.3:p.Trp255Ser
NM_004994.2:c.764G>C	NP_004985.2:p.Trp255Ser
NM_004994.3:c.764G>C MANE Select	NP_004985.2:p.Trp255Ser