Canonical Allele Identifier: CA977658665
Gene: MT2A HGNC NCBI

Linked Data

dbSNP Id: rs1960008489

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56609446A>G , CM000678.2:g.56609446A>G GRCh38
NC_000016.9:g.56643358A>G , CM000678.1:g.56643358A>G GRCh37
NC_000016.8:g.55200859A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000245185.6:c.*92A>G MANE Select ENSP00000245185.5:n.*92A>G
ENST00000245185.5:c.*92A>G ENSP00000245185.5:n.*92A>G
ENST00000561491.1:c.*261A>G ENSP00000456804.1:n.*261A>G
ENST00000562017.1:n.852A>G
ENST00000563985.1:n.658A>G
ENST00000567300.1:n.365A>G
NM_005953.3:c.*92A>G NP_005944.1:n.*92A>G
XR_933616.1:n.1044T>C
NM_005953.4:c.*92A>G NP_005944.1:n.*92A>G
NM_005953.5:c.*92A>G MANE Select NP_005944.1:n.*92A>G