Canonical Allele Identifier: CA510650641
Gene: MMP9 HGNC NCBI
SLC12A5-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.44644941T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46016302T>C , CM000682.2:g.46016302T>C GRCh38
NC_000020.10:g.44644941T>C , CM000682.1:g.44644941T>C GRCh37
NC_000020.9:g.44078348T>C NCBI36
NG_011468.1:g.12395T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.2058T>C (MMP9) MANE Select ENSP00000361405.3:p.Ser686=
NM_004994.2:c.2058T>C (MMP9) NP_004985.2:p.Ser686=
NR_147699.1:n.669-1514A>G (SLC12A5-AS1)
NM_004994.3:c.2058T>C (MMP9) MANE Select NP_004985.2:p.Ser686=