Canonical Allele Identifier: CA409228135
Gene: MMP9 HGNC NCBI
SLC12A5-AS1 HGNC NCBI

Linked Data

gnomAD v4: 20-46016337-C-T
MyVariant Identifiers: chr20:g.44644976C>T (hg19) chr20:g.46016337C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46016337C>T , CM000682.2:g.46016337C>T GRCh38
NC_000020.10:g.44644976C>T , CM000682.1:g.44644976C>T GRCh37
NC_000020.9:g.44078383C>T NCBI36
NG_011468.1:g.12430C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000372330.3:c.2093C>T (MMP9) MANE Select ENSP00000361405.3:p.Thr698Ile
NM_004994.2:c.2093C>T (MMP9) NP_004985.2:p.Thr698Ile
NR_147699.1:n.669-1549G>A (SLC12A5-AS1)
NM_004994.3:c.2093C>T (MMP9) MANE Select NP_004985.2:p.Thr698Ile
Search 100 bp 5'
Search 100 bp 3'