Canonical Allele Identifier: CA315634808

Gene: MMP9

Linked Data

• dbSNP Id: rs769270769
• gnomAD v2: 20-44639584-G-T
• gnomAD v4: 20-46010945-G-T
• MyVariant Identifiers: chr20:g.44639584G>T (hg19) ; chr20:g.46010945G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46010945G>T , CM000682.2:g.46010945G>T	GRCh38
NC_000020.10:g.44639584G>T , CM000682.1:g.44639584G>T	GRCh37
NC_000020.9:g.44072991G>T	NCBI36
NG_011468.1:g.7038G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372330.3:c.544G>T MANE Select	ENSP00000361405.3:p.Asp182Tyr
NM_004994.2:c.544G>T	NP_004985.2:p.Asp182Tyr
NM_004994.3:c.544G>T MANE Select	NP_004985.2:p.Asp182Tyr