Canonical Allele Identifier: CA382236665
Gene: MMP12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.102737999A>T (hg19) chr11:g.102867268A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102867268A>T , CM000673.2:g.102867268A>T GRCh38
NC_000011.9:g.102737999A>T , CM000673.1:g.102737999A>T GRCh37
NC_000011.8:g.102243209A>T NCBI36
NG_032936.1:g.12767T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000571244.3:c.911+2T>A MANE Select ENSP00000458585.1:n.911+2T>A
ENST00000571244.2:c.911+2T>A ENSP00000458585.1:n.911+2T>A
NM_002426.4:c.911+2T>A NP_002417.2:n.911+2T>A
NM_002426.5:c.911+2T>A NP_002417.2:n.911+2T>A
NM_002426.6:c.911+2T>A MANE Select NP_002417.2:n.911+2T>A
Search 100 bp 5'
Search 100 bp 3'