Canonical Allele Identifier: CA1135842212
Gene: TIMM8A HGNC NCBI

Linked Data

dbSNP Id: rs1926164313

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348948A>G , CM000685.2:g.101348948A>G GRCh38
NC_000023.10:g.100603936A>G , CM000685.1:g.100603936A>G GRCh37
NC_000023.9:g.100490592A>G NCBI36
NG_009616.1:g.42277T>C , LRG_128:g.42277T>C
NG_011734.1:g.5022T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.3:c.-284T>C ENSP00000361993.3:n.-284T>C
NM_004085.3:c.-284T>C NP_004076.1:n.-284T>C