Canonical Allele Identifier: CA382236754
Gene: MMP12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.102738040A>C (hg19) chr11:g.102867309A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102867309A>C , CM000673.2:g.102867309A>C GRCh38
NC_000011.9:g.102738040A>C , CM000673.1:g.102738040A>C GRCh37
NC_000011.8:g.102243250A>C NCBI36
NG_032936.1:g.12726T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000571244.3:c.872T>G MANE Select ENSP00000458585.1:p.Val291Gly
ENST00000571244.2:c.872T>G ENSP00000458585.1:p.Val291Gly
NM_002426.4:c.872T>G NP_002417.2:p.Val291Gly
NM_002426.5:c.872T>G NP_002417.2:p.Val291Gly
NM_002426.6:c.872T>G MANE Select NP_002417.2:p.Val291Gly
Search 100 bp 5'
Search 100 bp 3'