Canonical Allele Identifier: CA409214553

Gene: MMP9

Linked Data

• dbSNP Id: rs1239188179
• gnomAD v4: 20-46011592-G-C
• MyVariant Identifiers: chr20:g.44640231G>C (hg19) ; chr20:g.46011592G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46011592G>C , CM000682.2:g.46011592G>C	GRCh38
NC_000020.10:g.44640231G>C , CM000682.1:g.44640231G>C	GRCh37
NC_000020.9:g.44073638G>C	NCBI36
NG_011468.1:g.7685G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000372330.3:c.842G>C MANE Select	ENSP00000361405.3:p.Gly281Ala
NM_004994.2:c.842G>C	NP_004985.2:p.Gly281Ala
NM_004994.3:c.842G>C MANE Select	NP_004985.2:p.Gly281Ala