Canonical Allele Identifier: CA2224227363
Gene: MT2A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56609262G= , CM000678.2:g.56609262G= GRCh38
NC_000016.9:g.56643174G= , CM000678.1:g.56643174G= GRCh37
NC_000016.8:g.55200675G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000245185.6:c.95-1G= MANE Select ENSP00000245185.5:n.95-1G=
ENST00000245185.5:c.95-1G= ENSP00000245185.5:n.95-1G=
ENST00000561491.1:c.*77G= ENSP00000456804.1:n.*77G=
ENST00000562017.1:n.668G=
ENST00000563985.1:n.475-1G=
ENST00000567300.1:n.182-1G=
NM_005953.3:c.95-1G= NP_005944.1:n.95-1G=
NM_005953.4:c.95-1G= NP_005944.1:n.95-1G=
NM_005953.5:c.95-1G= MANE Select NP_005944.1:n.95-1G=
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