Canonical Allele Identifier: CA382236670
Gene: MMP12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.102738001C>A (hg19) chr11:g.102867270C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102867270C>A , CM000673.2:g.102867270C>A GRCh38
NC_000011.9:g.102738001C>A , CM000673.1:g.102738001C>A GRCh37
NC_000011.8:g.102243211C>A NCBI36
NG_032936.1:g.12765G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000571244.3:c.911G>T MANE Select ENSP00000458585.1:p.Arg304Met
ENST00000571244.2:c.911G>T ENSP00000458585.1:p.Arg304Met
NM_002426.4:c.911G>T NP_002417.2:p.Arg304Met
NM_002426.5:c.911G>T NP_002417.2:p.Arg304Met
NM_002426.6:c.911G>T MANE Select NP_002417.2:p.Arg304Met
Search 100 bp 5'
Search 100 bp 3'