Canonical Allele Identifier: CA2448281613
Gene: TIMM8A HGNC NCBI

Linked Data

dbSNP Id: rs1602997396

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348910C>G , CM000685.2:g.101348910C>G GRCh38
NC_000023.10:g.100603898C>G , CM000685.1:g.100603898C>G GRCh37
NC_000023.9:g.100490554C>G NCBI36
NG_009616.1:g.42315G>C , LRG_128:g.42315G>C
NG_011734.1:g.5060G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.3:c.-246G>C ENSP00000361993.3:n.-246G>C
NM_004085.3:c.-246G>C NP_004076.1:n.-246G>C