Canonical Allele Identifier: CA2615732094
Gene: MMP12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102867262G>A , CM000673.2:g.102867262G>A GRCh38
NC_000011.9:g.102737993G>A , CM000673.1:g.102737993G>A GRCh37
NC_000011.8:g.102243203G>A NCBI36
NG_032936.1:g.12773C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000571244.3:c.911+8C>T MANE Select ENSP00000458585.1:n.911+8C>T
ENST00000571244.2:c.911+8C>T ENSP00000458585.1:n.911+8C>T
NM_002426.4:c.911+8C>T NP_002417.2:n.911+8C>T
NM_002426.5:c.911+8C>T NP_002417.2:n.911+8C>T
NM_002426.6:c.911+8C>T MANE Select NP_002417.2:n.911+8C>T