Canonical Allele Identifier: CA322577421
Gene: MMP11 HGNC NCBI

Linked Data

dbSNP Id: rs994584220
gnomAD v3: 22-23771278-C-G
gnomAD v4: 22-23771278-C-G
MyVariant Identifiers: chr22:g.24113465C>G (hg19) chr22:g.23771278C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23771278C>G , CM000684.2:g.23771278C>G GRCh38
NC_000022.10:g.24113465C>G , CM000684.1:g.24113465C>G GRCh37
NC_000022.9:g.22443465C>G NCBI36
NG_029443.1:g.3430C>G
NG_034223.1:g.1695G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000465385.5:n.729C>G
ENST00000477567.5:n.243C>G
ENST00000489582.5:n.134+2485C>G
XR_001755453.1:n.729C>G
XR_001755454.1:n.729C>G
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