Canonical Allele Identifier: CA476582315
Gene: MMP12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.102733821T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102863090T>G , CM000673.2:g.102863090T>G GRCh38
NC_000011.9:g.102733821T>G , CM000673.1:g.102733821T>G GRCh37
NC_000011.8:g.102239031T>G NCBI36
NG_032936.1:g.16945A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000571244.3:c.*10A>C MANE Select ENSP00000458585.1:n.*10A>C
ENST00000571244.2:c.*10A>C ENSP00000458585.1:n.*10A>C
NM_002426.4:c.*10A>C NP_002417.2:n.*10A>C
NM_002426.5:c.*10A>C NP_002417.2:n.*10A>C
NM_002426.6:c.*10A>C MANE Select NP_002417.2:n.*10A>C
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