Canonical Allele Identifier: CA476582295
Gene: MMP12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.102733815A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102863084A>C , CM000673.2:g.102863084A>C GRCh38
NC_000011.9:g.102733815A>C , CM000673.1:g.102733815A>C GRCh37
NC_000011.8:g.102239025A>C NCBI36
NG_032936.1:g.16951T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000571244.3:c.*16T>G MANE Select ENSP00000458585.1:n.*16T>G
ENST00000571244.2:c.*16T>G ENSP00000458585.1:n.*16T>G
NM_002426.4:c.*16T>G NP_002417.2:n.*16T>G
NM_002426.5:c.*16T>G NP_002417.2:n.*16T>G
NM_002426.6:c.*16T>G MANE Select NP_002417.2:n.*16T>G