Canonical Allele Identifier: CA9886486
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs780627387
ExAC: 20:44639816 G / T
gnomAD v2: 20-44639816-G-T
gnomAD v4: 20-46011177-G-T
MyVariant Identifiers: chr20:g.44639816G>T (hg19) chr20:g.46011177G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46011177G>T , CM000682.2:g.46011177G>T GRCh38
NC_000020.10:g.44639816G>T , CM000682.1:g.44639816G>T GRCh37
NC_000020.9:g.44073223G>T NCBI36
NG_011468.1:g.7270G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.684G>T MANE Select ENSP00000361405.3:p.Ala228=
NM_004994.2:c.684G>T NP_004985.2:p.Ala228=
NM_004994.3:c.684G>T MANE Select NP_004985.2:p.Ala228=
Search 100 bp 5'
Search 100 bp 3'