Canonical Allele Identifier: CA721980231
Gene: MT2A HGNC NCBI

Linked Data

dbSNP Id: rs1424593992
MyVariant Identifiers: chr16:g.56643398G>A (hg19) chr16:g.56609486G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56609486G>A , CM000678.2:g.56609486G>A GRCh38
NC_000016.9:g.56643398G>A , CM000678.1:g.56643398G>A GRCh37
NC_000016.8:g.55200899G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000245185.6:c.*132G>A MANE Select ENSP00000245185.5:n.*132G>A
ENST00000245185.5:c.*132G>A ENSP00000245185.5:n.*132G>A
ENST00000561491.1:c.*301G>A ENSP00000456804.1:n.*301G>A
ENST00000562017.1:n.892G>A
ENST00000567300.1:n.405G>A
NM_005953.3:c.*132G>A NP_005944.1:n.*132G>A
XR_933616.1:n.1004C>T
NM_005953.4:c.*132G>A NP_005944.1:n.*132G>A
NM_005953.5:c.*132G>A MANE Select NP_005944.1:n.*132G>A
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