Canonical Allele Identifier: CA409211909
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs1162424705
gnomAD v2: 20-44638598-C-G
gnomAD v4: 20-46009959-C-G
MyVariant Identifiers: chr20:g.44638598C>G (hg19) chr20:g.46009959C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46009959C>G , CM000682.2:g.46009959C>G GRCh38
NC_000020.10:g.44638598C>G , CM000682.1:g.44638598C>G GRCh37
NC_000020.9:g.44072005C>G NCBI36
NG_011468.1:g.6052C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.232C>G MANE Select ENSP00000361405.3:p.Leu78Val
NM_004994.2:c.232C>G NP_004985.2:p.Leu78Val
NM_004994.3:c.232C>G MANE Select NP_004985.2:p.Leu78Val
Search 100 bp 5'
Search 100 bp 3'