Canonical Allele Identifier: CA2655693758
Gene: MMP11 HGNC NCBI

Linked Data

gnomAD v4: 22-23771267-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23771267T>C , CM000684.2:g.23771267T>C GRCh38
NC_000022.10:g.24113454T>C , CM000684.1:g.24113454T>C GRCh37
NC_000022.9:g.22443454T>C NCBI36
NG_029443.1:g.3419T>C
NG_034223.1:g.1706A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000465385.5:n.718T>C
ENST00000477567.5:n.232T>C
ENST00000489582.5:n.134+2474T>C
XR_001755453.1:n.718T>C
XR_001755454.1:n.718T>C
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