Canonical Allele Identifier: CA2633346754
Gene: MT2A HGNC NCBI

Linked Data

gnomAD v4: 16-56609451-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56609451T>A , CM000678.2:g.56609451T>A GRCh38
NC_000016.9:g.56643363T>A , CM000678.1:g.56643363T>A GRCh37
NC_000016.8:g.55200864T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000245185.6:c.*97T>A MANE Select ENSP00000245185.5:n.*97T>A
ENST00000245185.5:c.*97T>A ENSP00000245185.5:n.*97T>A
ENST00000561491.1:c.*266T>A ENSP00000456804.1:n.*266T>A
ENST00000562017.1:n.857T>A
ENST00000563985.1:n.663T>A
ENST00000567300.1:n.370T>A
NM_005953.3:c.*97T>A NP_005944.1:n.*97T>A
XR_933616.1:n.1039A>T
NM_005953.4:c.*97T>A NP_005944.1:n.*97T>A
NM_005953.5:c.*97T>A MANE Select NP_005944.1:n.*97T>A
Search 100 bp 5'
Search 100 bp 3'