Canonical Allele Identifier: CA395964395
Gene: MT2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56609344G>T , CM000678.2:g.56609344G>T GRCh38
NC_000016.9:g.56643256G>T , CM000678.1:g.56643256G>T GRCh37
NC_000016.8:g.55200757G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000245185.6:c.176G>T MANE Select ENSP00000245185.5:p.Cys59Phe
ENST00000245185.5:c.176G>T ENSP00000245185.5:p.Cys59Phe
ENST00000561491.1:c.*159G>T ENSP00000456804.1:n.*159G>T
ENST00000562017.1:n.750G>T
ENST00000563985.1:n.556G>T
ENST00000567300.1:n.263G>T
NM_005953.3:c.176G>T NP_005944.1:p.Cys59Phe
NM_005953.4:c.176G>T NP_005944.1:p.Cys59Phe
NM_005953.5:c.176G>T MANE Select NP_005944.1:p.Cys59Phe