Canonical Allele Identifier: CA395963881
Gene: MT2A HGNC NCBI

Linked Data

dbSNP Id: rs1567338091
MyVariant Identifiers: chr16:g.56643175G>C (hg19) chr16:g.56609263G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56609263G>C , CM000678.2:g.56609263G>C GRCh38
NC_000016.9:g.56643175G>C , CM000678.1:g.56643175G>C GRCh37
NC_000016.8:g.55200676G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000245185.6:c.95G>C MANE Select ENSP00000245185.5:p.Ser32Thr
ENST00000245185.5:c.95G>C ENSP00000245185.5:p.Ser32Thr
ENST00000561491.1:c.*78G>C ENSP00000456804.1:n.*78G>C
ENST00000562017.1:n.669G>C
ENST00000563985.1:n.475G>C
ENST00000567300.1:n.182G>C
NM_005953.3:c.95G>C NP_005944.1:p.Ser32Thr
NM_005953.4:c.95G>C NP_005944.1:p.Ser32Thr
NM_005953.5:c.95G>C MANE Select NP_005944.1:p.Ser32Thr
Search 100 bp 5'
Search 100 bp 3'