Canonical Allele Identifier: CA9886523
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs774058590
ExAC: 20:44639994 C / G
gnomAD v2: 20-44639994-C-G
gnomAD v4: 20-46011355-C-G
MyVariant Identifiers: chr20:g.44639994C>G (hg19) chr20:g.46011355C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011355C>G , CM000682.2:g.46011355C>G GRCh38
NC_000020.10:g.44639994C>G , CM000682.1:g.44639994C>G GRCh37
NC_000020.9:g.44073401C>G NCBI36
NG_011468.1:g.7448C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.823+39C>G MANE Select ENSP00000361405.3:n.823+39C>G
NM_004994.2:c.823+39C>G NP_004985.2:n.823+39C>G
NM_004994.3:c.823+39C>G MANE Select NP_004985.2:n.823+39C>G
Search 100 bp 5'
Search 100 bp 3'