Canonical Allele Identifier: CA1996274283
Gene: MMP12 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102867267T= , CM000673.2:g.102867267T= GRCh38
NC_000011.9:g.102737998T= , CM000673.1:g.102737998T= GRCh37
NC_000011.8:g.102243208T= NCBI36
NG_032936.1:g.12768A=

Transcript Alleles

HGVS Amino-acid change
ENST00000571244.3:c.911+3A= MANE Select ENSP00000458585.1:n.911+3A=
ENST00000571244.2:c.911+3A= ENSP00000458585.1:n.911+3A=
NM_002426.4:c.911+3A= NP_002417.2:n.911+3A=
NM_002426.5:c.911+3A= NP_002417.2:n.911+3A=
NM_002426.6:c.911+3A= MANE Select NP_002417.2:n.911+3A=
Search 100 bp 5'
Search 100 bp 3'