Canonical Allele Identifier: CA751790443
Gene: MMP11 HGNC NCBI

Linked Data

dbSNP Id: rs1337951578
gnomAD v3: 22-23771260-G-T
gnomAD v4: 22-23771260-G-T
MyVariant Identifiers: chr22:g.24113447G>T (hg19) chr22:g.23771260G>T (hg38)
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Genomic Alleles

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

Transcript Alleles

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