Canonical Allele Identifier: CA476582299
Gene: MMP12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.102733816T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102863085T>C , CM000673.2:g.102863085T>C GRCh38
NC_000011.9:g.102733816T>C , CM000673.1:g.102733816T>C GRCh37
NC_000011.8:g.102239026T>C NCBI36
NG_032936.1:g.16950A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000571244.3:c.*15A>G MANE Select ENSP00000458585.1:n.*15A>G
ENST00000571244.2:c.*15A>G ENSP00000458585.1:n.*15A>G
NM_002426.4:c.*15A>G NP_002417.2:n.*15A>G
NM_002426.5:c.*15A>G NP_002417.2:n.*15A>G
NM_002426.6:c.*15A>G MANE Select NP_002417.2:n.*15A>G