Canonical Allele Identifier: CA382236775
Gene: MMP12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.102738049A>T (hg19) chr11:g.102867318A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102867318A>T , CM000673.2:g.102867318A>T GRCh38
NC_000011.9:g.102738049A>T , CM000673.1:g.102738049A>T GRCh37
NC_000011.8:g.102243259A>T NCBI36
NG_032936.1:g.12717T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000571244.3:c.863T>A MANE Select ENSP00000458585.1:p.Phe288Tyr
ENST00000571244.2:c.863T>A ENSP00000458585.1:p.Phe288Tyr
NM_002426.4:c.863T>A NP_002417.2:p.Phe288Tyr
NM_002426.5:c.863T>A NP_002417.2:p.Phe288Tyr
NM_002426.6:c.863T>A MANE Select NP_002417.2:p.Phe288Tyr
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