Canonical Allele Identifier: CA636176585
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs1378985271
gnomAD v2: 20-44639984-G-T
gnomAD v4: 20-46011345-G-T
MyVariant Identifiers: chr20:g.44639984G>T (hg19) chr20:g.46011345G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011345G>T , CM000682.2:g.46011345G>T GRCh38
NC_000020.10:g.44639984G>T , CM000682.1:g.44639984G>T GRCh37
NC_000020.9:g.44073391G>T NCBI36
NG_011468.1:g.7438G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.823+29G>T MANE Select ENSP00000361405.3:n.823+29G>T
NM_004994.2:c.823+29G>T NP_004985.2:n.823+29G>T
NM_004994.3:c.823+29G>T MANE Select NP_004985.2:n.823+29G>T
Search 100 bp 5'
Search 100 bp 3'