Canonical Allele Identifier: CA2615732077
Gene: MMP12 HGNC NCBI

Linked Data

gnomAD v4: 11-102867252-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102867252A>T , CM000673.2:g.102867252A>T GRCh38
NC_000011.9:g.102737983A>T , CM000673.1:g.102737983A>T GRCh37
NC_000011.8:g.102243193A>T NCBI36
NG_032936.1:g.12783T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000571244.3:c.911+18T>A MANE Select ENSP00000458585.1:n.911+18T>A
ENST00000571244.2:c.911+18T>A ENSP00000458585.1:n.911+18T>A
NM_002426.4:c.911+18T>A NP_002417.2:n.911+18T>A
NM_002426.5:c.911+18T>A NP_002417.2:n.911+18T>A
NM_002426.6:c.911+18T>A MANE Select NP_002417.2:n.911+18T>A
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