Canonical Allele Identifier: CA476582322
Gene: MMP12 HGNC NCBI

Linked Data

gnomAD v4: 11-102863093-A-T
MyVariant Identifiers: chr11:g.102733824A>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102863093A>T , CM000673.2:g.102863093A>T GRCh38
NC_000011.9:g.102733824A>T , CM000673.1:g.102733824A>T GRCh37
NC_000011.8:g.102239034A>T NCBI36
NG_032936.1:g.16942T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000571244.3:c.*7T>A MANE Select ENSP00000458585.1:n.*7T>A
ENST00000571244.2:c.*7T>A ENSP00000458585.1:n.*7T>A
NM_002426.4:c.*7T>A NP_002417.2:n.*7T>A
NM_002426.5:c.*7T>A NP_002417.2:n.*7T>A
NM_002426.6:c.*7T>A MANE Select NP_002417.2:n.*7T>A
Search 100 bp 5'
Search 100 bp 3'