Canonical Allele Identifier: CA2397951110
Gene: MMP11 HGNC NCBI

Linked Data

dbSNP Id: rs1337951578

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23771260G>A , CM000684.2:g.23771260G>A GRCh38
NC_000022.10:g.24113447G>A , CM000684.1:g.24113447G>A GRCh37
NC_000022.9:g.22443447G>A NCBI36
NG_029443.1:g.3412G>A
NG_034223.1:g.1713C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000465385.5:n.711G>A
ENST00000477567.5:n.225G>A
ENST00000489582.5:n.134+2467G>A
XR_001755453.1:n.711G>A
XR_001755454.1:n.711G>A