Canonical Allele Identifier: CA2448281649
Gene: TIMM8A HGNC NCBI

Linked Data

dbSNP Id: rs1926168311

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348991dup , CM000685.2:g.101348991dup GRCh38
NC_000023.10:g.100603979dup , CM000685.1:g.100603979dup GRCh37
NC_000023.9:g.100490635dup NCBI36
NG_009616.1:g.42236dup , LRG_128:g.42236dup
NG_011734.1:g.4981dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.3:c.-325dup ENSP00000361993.3:n.-325dup