Canonical Allele Identifier: CA751790462
Gene: MMP11 HGNC NCBI

Linked Data

dbSNP Id: rs1402462225
gnomAD v3: 22-23771289-C-A
gnomAD v4: 22-23771289-C-A
MyVariant Identifiers: chr22:g.24113476C>A (hg19) chr22:g.23771289C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23771289C>A , CM000684.2:g.23771289C>A GRCh38
NC_000022.10:g.24113476C>A , CM000684.1:g.24113476C>A GRCh37
NC_000022.9:g.22443476C>A NCBI36
NG_029443.1:g.3441C>A
NG_034223.1:g.1684G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000465385.5:n.740C>A
ENST00000477567.5:n.254C>A
ENST00000489582.5:n.134+2496C>A
XR_001755453.1:n.740C>A
XR_001755454.1:n.740C>A
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