Canonical Allele Identifier: CA2633346760
Gene: MT2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56609461A>G , CM000678.2:g.56609461A>G GRCh38
NC_000016.9:g.56643373A>G , CM000678.1:g.56643373A>G GRCh37
NC_000016.8:g.55200874A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000245185.6:c.*107A>G MANE Select ENSP00000245185.5:n.*107A>G
ENST00000245185.5:c.*107A>G ENSP00000245185.5:n.*107A>G
ENST00000561491.1:c.*276A>G ENSP00000456804.1:n.*276A>G
ENST00000562017.1:n.867A>G
ENST00000563985.1:n.673A>G
ENST00000567300.1:n.380A>G
NM_005953.3:c.*107A>G NP_005944.1:n.*107A>G
XR_933616.1:n.1029T>C
NM_005953.4:c.*107A>G NP_005944.1:n.*107A>G
NM_005953.5:c.*107A>G MANE Select NP_005944.1:n.*107A>G