Canonical Allele Identifier: CA9886481
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs750293045
ExAC: 20:44639790 A / G
gnomAD v2: 20-44639790-A-G
gnomAD v3: 20-46011151-A-G
gnomAD v4: 20-46011151-A-G
MyVariant Identifiers: chr20:g.44639790A>G (hg19) chr20:g.46011151A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011151A>G , CM000682.2:g.46011151A>G GRCh38
NC_000020.10:g.44639790A>G , CM000682.1:g.44639790A>G GRCh37
NC_000020.9:g.44073197A>G NCBI36
NG_011468.1:g.7244A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.658A>G MANE Select ENSP00000361405.3:p.Thr220Ala
NM_004994.2:c.658A>G NP_004985.2:p.Thr220Ala
NM_004994.3:c.658A>G MANE Select NP_004985.2:p.Thr220Ala
Search 100 bp 5'
Search 100 bp 3'