Canonical Allele Identifier: CA315635312
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs35573488
MyVariant Identifiers: chr20:g.44640230_44640231insA (hg19) chr20:g.46011591_46011592insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011591_46011592insA , CM000682.2:g.46011591_46011592insA GRCh38
NC_000020.10:g.44640230_44640231insA , CM000682.1:g.44640230_44640231insA GRCh37
NC_000020.9:g.44073637_44073638insA NCBI36
NG_011468.1:g.7684_7685insA

Transcript Alleles

HGVS Amino-acid change
ENST00000372330.3:c.841_842insA MANE Select ENSP00000361405.3:p.Gly281GlufsTer4
NM_004994.2:c.841_842insA NP_004985.2:p.Gly281GlufsTer4
NM_004994.3:c.841_842insA MANE Select NP_004985.2:p.Gly281GlufsTer4
Search 100 bp 5'
Search 100 bp 3'