Canonical Allele Identifier: CA2448281631
Gene: TIMM8A HGNC NCBI

Linked Data

dbSNP Id: rs1926164164

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348947C>G , CM000685.2:g.101348947C>G GRCh38
NC_000023.10:g.100603935C>G , CM000685.1:g.100603935C>G GRCh37
NC_000023.9:g.100490591C>G NCBI36
NG_009616.1:g.42278G>C , LRG_128:g.42278G>C
NG_011734.1:g.5023G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.3:c.-283G>C ENSP00000361993.3:n.-283G>C
NM_004085.3:c.-283G>C NP_004076.1:n.-283G>C