Canonical Allele Identifier: CA2633346769
Gene: MT2A HGNC NCBI

Linked Data

gnomAD v4: 16-56609480-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56609480A>G , CM000678.2:g.56609480A>G GRCh38
NC_000016.9:g.56643392A>G , CM000678.1:g.56643392A>G GRCh37
NC_000016.8:g.55200893A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000245185.6:c.*126A>G MANE Select ENSP00000245185.5:n.*126A>G
ENST00000245185.5:c.*126A>G ENSP00000245185.5:n.*126A>G
ENST00000561491.1:c.*295A>G ENSP00000456804.1:n.*295A>G
ENST00000562017.1:n.886A>G
ENST00000567300.1:n.399A>G
NM_005953.3:c.*126A>G NP_005944.1:n.*126A>G
XR_933616.1:n.1010T>C
NM_005953.4:c.*126A>G NP_005944.1:n.*126A>G
NM_005953.5:c.*126A>G MANE Select NP_005944.1:n.*126A>G
Search 100 bp 5'
Search 100 bp 3'