Canonical Allele Identifier: CA2738824000
Gene: TIMM8A HGNC NCBI

Linked Data

dbSNP Id: rs2147418627

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348955A>C , CM000685.2:g.101348955A>C GRCh38
NC_000023.10:g.100603943A>C , CM000685.1:g.100603943A>C GRCh37
NC_000023.9:g.100490599A>C NCBI36
NG_009616.1:g.42270T>G , LRG_128:g.42270T>G
NG_011734.1:g.5015T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.3:c.-291T>G ENSP00000361993.3:n.-291T>G
NM_004085.3:c.-291T>G NP_004076.1:n.-291T>G