Canonical Allele Identifier: CA601219210
Gene: MMP12 HGNC NCBI

Linked Data

dbSNP Id: rs1555008675
gnomAD v2: 11-102737975-T-C
gnomAD v3: 11-102867244-T-C
gnomAD v4: 11-102867244-T-C
MyVariant Identifiers: chr11:g.102737975T>C (hg19) chr11:g.102867244T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102867244T>C , CM000673.2:g.102867244T>C GRCh38
NC_000011.9:g.102737975T>C , CM000673.1:g.102737975T>C GRCh37
NC_000011.8:g.102243185T>C NCBI36
NG_032936.1:g.12791A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000571244.3:c.911+26A>G MANE Select ENSP00000458585.1:n.911+26A>G
ENST00000571244.2:c.911+26A>G ENSP00000458585.1:n.911+26A>G
NM_002426.4:c.911+26A>G NP_002417.2:n.911+26A>G
NM_002426.5:c.911+26A>G NP_002417.2:n.911+26A>G
NM_002426.6:c.911+26A>G MANE Select NP_002417.2:n.911+26A>G
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