Canonical Allele Identifier: CA2655693778
Gene: MMP11 HGNC NCBI

Linked Data

gnomAD v4: 22-23771283-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23771283A>G , CM000684.2:g.23771283A>G GRCh38
NC_000022.10:g.24113470A>G , CM000684.1:g.24113470A>G GRCh37
NC_000022.9:g.22443470A>G NCBI36
NG_029443.1:g.3435A>G
NG_034223.1:g.1690T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000465385.5:n.734A>G
ENST00000477567.5:n.248A>G
ENST00000489582.5:n.134+2490A>G
XR_001755453.1:n.734A>G
XR_001755454.1:n.734A>G
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