Canonical Allele Identifier: CA476582300
Gene: MMP12 HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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