Canonical Allele Identifier: CA601219214
Gene: MMP12 HGNC NCBI

Linked Data

dbSNP Id: rs1472403712
gnomAD v2: 11-102737996-C-A
gnomAD v3: 11-102867265-C-A
gnomAD v4: 11-102867265-C-A
MyVariant Identifiers: chr11:g.102737996C>A (hg19) chr11:g.102867265C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102867265C>A , CM000673.2:g.102867265C>A GRCh38
NC_000011.9:g.102737996C>A , CM000673.1:g.102737996C>A GRCh37
NC_000011.8:g.102243206C>A NCBI36
NG_032936.1:g.12770G>T

Transcript Alleles

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