Canonical Allele Identifier: CA476582329

Gene: MMP12

Linked Data

• MyVariant Identifiers: chr11:g.102733826C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102863095C>G , CM000673.2:g.102863095C>G	GRCh38
NC_000011.9:g.102733826C>G , CM000673.1:g.102733826C>G	GRCh37
NC_000011.8:g.102239036C>G	NCBI36
NG_032936.1:g.16940G>C

Transcript Alleles

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