Canonical Allele Identifier: CA510642667
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs2145453206
gnomAD v4: 20-46011743-C-T
MyVariant Identifiers: chr20:g.44640382C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011743C>T , CM000682.2:g.46011743C>T GRCh38
NC_000020.10:g.44640382C>T , CM000682.1:g.44640382C>T GRCh37
NC_000020.9:g.44073789C>T NCBI36
NG_011468.1:g.7836C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.993C>T MANE Select ENSP00000361405.3:p.Thr331=
NM_004994.2:c.993C>T NP_004985.2:p.Thr331=
NM_004994.3:c.993C>T MANE Select NP_004985.2:p.Thr331=
Search 100 bp 5'
Search 100 bp 3'