Canonical Allele Identifier: CA382236667
Gene: MMP12 HGNC NCBI

Linked Data

gnomAD v4: 11-102867269-C-G
MyVariant Identifiers: chr11:g.102738000C>G (hg19) chr11:g.102867269C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102867269C>G , CM000673.2:g.102867269C>G GRCh38
NC_000011.9:g.102738000C>G , CM000673.1:g.102738000C>G GRCh37
NC_000011.8:g.102243210C>G NCBI36
NG_032936.1:g.12766G>C

Transcript Alleles

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