Canonical Allele Identifier: CA2738824105
Gene: TIMM8A HGNC NCBI

Linked Data

dbSNP Id: rs2147418653

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348977del , CM000685.2:g.101348977del GRCh38
NC_000023.10:g.100603965del , CM000685.1:g.100603965del GRCh37
NC_000023.9:g.100490621del NCBI36
NG_009616.1:g.42249del , LRG_128:g.42249del
NG_011734.1:g.4994del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.3:c.-312del ENSP00000361993.3:n.-312del