Canonical Allele Identifier: CA2448281644
Gene: TIMM8A HGNC NCBI

Linked Data

dbSNP Id: rs1926166300

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348989_101349000del , CM000685.2:g.101348989_101349000del GRCh38
NC_000023.10:g.100603977_100603988del , CM000685.1:g.100603977_100603988del GRCh37
NC_000023.9:g.100490633_100490644del NCBI36
NG_009616.1:g.42232_42243del , LRG_128:g.42232_42243del
NG_011734.1:g.4977_4988del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.3:c.-329_-318del ENSP00000361993.3:n.-329_-318del