Canonical Allele Identifier: CA2633346741
Gene: MT2A HGNC NCBI

Linked Data

dbSNP Id: rs2144292841

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56609436C>G , CM000678.2:g.56609436C>G GRCh38
NC_000016.9:g.56643348C>G , CM000678.1:g.56643348C>G GRCh37
NC_000016.8:g.55200849C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000245185.6:c.*82C>G MANE Select ENSP00000245185.5:n.*82C>G
ENST00000245185.5:c.*82C>G ENSP00000245185.5:n.*82C>G
ENST00000561491.1:c.*251C>G ENSP00000456804.1:n.*251C>G
ENST00000562017.1:n.842C>G
ENST00000563985.1:n.648C>G
ENST00000567300.1:n.355C>G
NM_005953.3:c.*82C>G NP_005944.1:n.*82C>G
XR_933616.1:n.1054G>C
NM_005953.4:c.*82C>G NP_005944.1:n.*82C>G
NM_005953.5:c.*82C>G MANE Select NP_005944.1:n.*82C>G