Canonical Allele Identifier: CA2655693775
Gene: MMP11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23771280A>G , CM000684.2:g.23771280A>G GRCh38
NC_000022.10:g.24113467A>G , CM000684.1:g.24113467A>G GRCh37
NC_000022.9:g.22443467A>G NCBI36
NG_029443.1:g.3432A>G
NG_034223.1:g.1693T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000465385.5:n.731A>G
ENST00000477567.5:n.245A>G
ENST00000489582.5:n.134+2487A>G
XR_001755453.1:n.731A>G
XR_001755454.1:n.731A>G