Canonical Allele Identifier: CA395963895
Gene: MT2A HGNC NCBI

Linked Data

gnomAD v4: 16-56609266-G-A
MyVariant Identifiers: chr16:g.56643178G>A (hg19) chr16:g.56609266G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56609266G>A , CM000678.2:g.56609266G>A GRCh38
NC_000016.9:g.56643178G>A , CM000678.1:g.56643178G>A GRCh37
NC_000016.8:g.55200679G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000245185.6:c.98G>A MANE Select ENSP00000245185.5:p.Cys33Tyr
ENST00000245185.5:c.98G>A ENSP00000245185.5:p.Cys33Tyr
ENST00000561491.1:c.*81G>A ENSP00000456804.1:n.*81G>A
ENST00000562017.1:n.672G>A
ENST00000563985.1:n.478G>A
ENST00000567300.1:n.185G>A
NM_005953.3:c.98G>A NP_005944.1:p.Cys33Tyr
NM_005953.4:c.98G>A NP_005944.1:p.Cys33Tyr
NM_005953.5:c.98G>A MANE Select NP_005944.1:p.Cys33Tyr
Search 100 bp 5'
Search 100 bp 3'