Canonical Allele Identifier: CA2655693780
Gene: MMP11 HGNC NCBI

Linked Data

gnomAD v4: 22-23771285-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23771285G>T , CM000684.2:g.23771285G>T GRCh38
NC_000022.10:g.24113472G>T , CM000684.1:g.24113472G>T GRCh37
NC_000022.9:g.22443472G>T NCBI36
NG_029443.1:g.3437G>T
NG_034223.1:g.1688C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000465385.5:n.736G>T
ENST00000477567.5:n.250G>T
ENST00000489582.5:n.134+2492G>T
XR_001755453.1:n.736G>T
XR_001755454.1:n.736G>T
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