Canonical Allele Identifier: CA476586276
Gene: MMP12 HGNC NCBI

Linked Data

dbSNP Id: rs571598878
gnomAD v4: 11-102867302-G-T
MyVariant Identifiers: chr11:g.102738033G>T (hg19) chr11:g.102867302G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102867302G>T , CM000673.2:g.102867302G>T GRCh38
NC_000011.9:g.102738033G>T , CM000673.1:g.102738033G>T GRCh37
NC_000011.8:g.102243243G>T NCBI36
NG_032936.1:g.12733C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000571244.3:c.879C>A MANE Select ENSP00000458585.1:p.Thr293=
ENST00000571244.2:c.879C>A ENSP00000458585.1:p.Thr293=
NM_002426.4:c.879C>A NP_002417.2:p.Thr293=
NM_002426.5:c.879C>A NP_002417.2:p.Thr293=
NM_002426.6:c.879C>A MANE Select NP_002417.2:p.Thr293=
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Search 100 bp 3'