Canonical Allele Identifier: CA409227985
Gene: MMP9 HGNC NCBI
SLC12A5-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2084322068
gnomAD v4: 20-46016321-C-T
MyVariant Identifiers: chr20:g.44644960C>T (hg19) chr20:g.46016321C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46016321C>T , CM000682.2:g.46016321C>T GRCh38
NC_000020.10:g.44644960C>T , CM000682.1:g.44644960C>T GRCh37
NC_000020.9:g.44078367C>T NCBI36
NG_011468.1:g.12414C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.2077C>T (MMP9) MANE Select ENSP00000361405.3:p.Gln693Ter
NM_004994.2:c.2077C>T (MMP9) NP_004985.2:p.Gln693Ter
NR_147699.1:n.669-1533G>A (SLC12A5-AS1)
NM_004994.3:c.2077C>T (MMP9) MANE Select NP_004985.2:p.Gln693Ter
Search 100 bp 5'
Search 100 bp 3'