Canonical Allele Identifier: CA2224227449
Gene: MT2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56609444A= , CM000678.2:g.56609444A= GRCh38
NC_000016.9:g.56643356A= , CM000678.1:g.56643356A= GRCh37
NC_000016.8:g.55200857A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000245185.6:c.*90A= MANE Select ENSP00000245185.5:n.*90A=
ENST00000245185.5:c.*90A= ENSP00000245185.5:n.*90A=
ENST00000561491.1:c.*259A= ENSP00000456804.1:n.*259A=
ENST00000562017.1:n.850A=
ENST00000563985.1:n.656A=
ENST00000567300.1:n.363A=
NM_005953.3:c.*90A= NP_005944.1:n.*90A=
XR_933616.1:n.1046T=
NM_005953.4:c.*90A= NP_005944.1:n.*90A=
NM_005953.5:c.*90A= MANE Select NP_005944.1:n.*90A=