Canonical Allele Identifier: CA751790448
Gene: MMP11 HGNC NCBI

Linked Data

dbSNP Id: rs1452583531

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23771266C>T , CM000684.2:g.23771266C>T GRCh38
NC_000022.10:g.24113453C>T , CM000684.1:g.24113453C>T GRCh37
NC_000022.9:g.22443453C>T NCBI36
NG_029443.1:g.3418C>T
NG_034223.1:g.1707G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000465385.5:n.717C>T
ENST00000477567.5:n.231C>T
ENST00000489582.5:n.134+2473C>T
XR_001755453.1:n.717C>T
XR_001755454.1:n.717C>T