Canonical Allele Identifier: CA2694293862
Gene: TIMM8A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348867C>A , CM000685.2:g.101348867C>A GRCh38
NC_000023.10:g.100603855C>A , CM000685.1:g.100603855C>A GRCh37
NC_000023.9:g.100490511C>A NCBI36
NG_009616.1:g.42358G>T , LRG_128:g.42358G>T
NG_011734.1:g.5103G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.3:c.-203G>T ENSP00000361993.3:n.-203G>T
NM_004085.3:c.-203G>T NP_004076.1:n.-203G>T