Canonical Allele Identifier: CA636176742
Gene: MMP9 HGNC NCBI

Linked Data

dbSNP Id: rs1332254991
gnomAD v2: 20-44639409-CAG-C
gnomAD v3: 20-46010770-CAG-C
gnomAD v4: 20-46010770-CAG-C
MyVariant Identifiers: chr20:g.44639410_44639411del (hg19) chr20:g.46010771_46010772del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46010772_46010773del , CM000682.2:g.46010772_46010773del GRCh38
NC_000020.10:g.44639411_44639412del , CM000682.1:g.44639411_44639412del GRCh37
NC_000020.9:g.44072818_44072819del NCBI36
NG_011468.1:g.6865_6866del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372330.3:c.520+141_520+142del MANE Select ENSP00000361405.3:n.520+141_520+142del
NM_004994.2:c.520+141_520+142del NP_004985.2:n.520+141_520+142del
NM_004994.3:c.520+141_520+142del MANE Select NP_004985.2:n.520+141_520+142del
Search 100 bp 5'
Search 100 bp 3'