Canonical Allele Identifier: CA476582328
Gene: MMP12 HGNC NCBI

Linked Data

gnomAD v4: 11-102863095-C-A
MyVariant Identifiers: chr11:g.102733826C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102863095C>A , CM000673.2:g.102863095C>A GRCh38
NC_000011.9:g.102733826C>A , CM000673.1:g.102733826C>A GRCh37
NC_000011.8:g.102239036C>A NCBI36
NG_032936.1:g.16940G>T

Transcript Alleles

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