Canonical Allele Identifier: CA751790447
Gene: MMP11 HGNC NCBI

Linked Data

dbSNP Id: rs1308295742
gnomAD v3: 22-23771261-T-G
gnomAD v4: 22-23771261-T-G
MyVariant Identifiers: chr22:g.24113448T>G (hg19) chr22:g.23771261T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23771261T>G , CM000684.2:g.23771261T>G GRCh38
NC_000022.10:g.24113448T>G , CM000684.1:g.24113448T>G GRCh37
NC_000022.9:g.22443448T>G NCBI36
NG_029443.1:g.3413T>G
NG_034223.1:g.1712A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000465385.5:n.712T>G
ENST00000477567.5:n.226T>G
ENST00000489582.5:n.134+2468T>G
XR_001755453.1:n.712T>G
XR_001755454.1:n.712T>G
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