Canonical Allele Identifier: CA395963889
Gene: MT2A HGNC NCBI

Linked Data

gnomAD v4: 16-56609265-T-A
MyVariant Identifiers: chr16:g.56643177T>A (hg19) chr16:g.56609265T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56609265T>A , CM000678.2:g.56609265T>A GRCh38
NC_000016.9:g.56643177T>A , CM000678.1:g.56643177T>A GRCh37
NC_000016.8:g.55200678T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000245185.6:c.97T>A MANE Select ENSP00000245185.5:p.Cys33Ser
ENST00000245185.5:c.97T>A ENSP00000245185.5:p.Cys33Ser
ENST00000561491.1:c.*80T>A ENSP00000456804.1:n.*80T>A
ENST00000562017.1:n.671T>A
ENST00000563985.1:n.477T>A
ENST00000567300.1:n.184T>A
NM_005953.3:c.97T>A NP_005944.1:p.Cys33Ser
NM_005953.4:c.97T>A NP_005944.1:p.Cys33Ser
NM_005953.5:c.97T>A MANE Select NP_005944.1:p.Cys33Ser
Search 100 bp 5'
Search 100 bp 3'