Canonical Allele Identifier: CA2615732063
Gene: MMP12 HGNC NCBI

Linked Data

gnomAD v4: 11-102867247-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102867247G>A , CM000673.2:g.102867247G>A GRCh38
NC_000011.9:g.102737978G>A , CM000673.1:g.102737978G>A GRCh37
NC_000011.8:g.102243188G>A NCBI36
NG_032936.1:g.12788C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000571244.3:c.911+23C>T MANE Select ENSP00000458585.1:n.911+23C>T
ENST00000571244.2:c.911+23C>T ENSP00000458585.1:n.911+23C>T
NM_002426.4:c.911+23C>T NP_002417.2:n.911+23C>T
NM_002426.5:c.911+23C>T NP_002417.2:n.911+23C>T
NM_002426.6:c.911+23C>T MANE Select NP_002417.2:n.911+23C>T
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