Canonical Allele Identifier: CA1024500825
Gene: MMP11 HGNC NCBI

Linked Data

dbSNP Id: rs1927187356

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23771275C>T , CM000684.2:g.23771275C>T GRCh38
NC_000022.10:g.24113462C>T , CM000684.1:g.24113462C>T GRCh37
NC_000022.9:g.22443462C>T NCBI36
NG_029443.1:g.3427C>T
NG_034223.1:g.1698G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000465385.5:n.726C>T
ENST00000477567.5:n.240C>T
ENST00000489582.5:n.134+2482C>T
XR_001755453.1:n.726C>T
XR_001755454.1:n.726C>T