Canonical Allele Identifier: CA2818529920
Gene: MMP11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23771258T>C , CM000684.2:g.23771258T>C GRCh38
NC_000022.10:g.24113445T>C , CM000684.1:g.24113445T>C GRCh37
NC_000022.9:g.22443445T>C NCBI36
NG_029443.1:g.3410T>C
NG_034223.1:g.1715A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000465385.5:n.709T>C
ENST00000477567.5:n.223T>C
ENST00000489582.5:n.134+2465T>C
XR_001755453.1:n.709T>C
XR_001755454.1:n.709T>C