Canonical Allele Identifier: CA2615732073
Gene: MMP12 HGNC NCBI

Linked Data

gnomAD v4: 11-102867250-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102867250A>G , CM000673.2:g.102867250A>G GRCh38
NC_000011.9:g.102737981A>G , CM000673.1:g.102737981A>G GRCh37
NC_000011.8:g.102243191A>G NCBI36
NG_032936.1:g.12785T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000571244.3:c.911+20T>C MANE Select ENSP00000458585.1:n.911+20T>C
ENST00000571244.2:c.911+20T>C ENSP00000458585.1:n.911+20T>C
NM_002426.4:c.911+20T>C NP_002417.2:n.911+20T>C
NM_002426.5:c.911+20T>C NP_002417.2:n.911+20T>C
NM_002426.6:c.911+20T>C MANE Select NP_002417.2:n.911+20T>C
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