ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA414822684
Gene: MT-ND6
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrMT:g.14482C>T
Linked Data - NCBI & NCI
dbSNP:
199476108
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.14482C>T , J01415.2:m.14482C>T
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361681.2:c.192G>A
ENSP00000354665.2:p.Met64Ile
Search 100 bp 5'
Search 100 bp 3'