Canonical Allele Identifier: CA315639487
Gene: MMP9 HGNC NCBI
SLC12A5-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1027492726
gnomAD v4: 20-46016113-G-T
MyVariant Identifiers: chr20:g.44644752G>T (hg19) chr20:g.46016113G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46016113G>T , CM000682.2:g.46016113G>T GRCh38
NC_000020.10:g.44644752G>T , CM000682.1:g.44644752G>T GRCh37
NC_000020.9:g.44078159G>T NCBI36
NG_011468.1:g.12206G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.2006-137G>T (MMP9) MANE Select ENSP00000361405.3:n.2006-137G>T
NM_004994.2:c.2006-137G>T (MMP9) NP_004985.2:n.2006-137G>T
NR_147699.1:n.669-1325C>A (SLC12A5-AS1)
NM_004994.3:c.2006-137G>T (MMP9) MANE Select NP_004985.2:n.2006-137G>T
Search 100 bp 5'
Search 100 bp 3'