Canonical Allele Identifier: CA2448281640
Gene: TIMM8A HGNC NCBI

Linked Data

dbSNP Id: rs1926165886

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348987_101348991del , CM000685.2:g.101348987_101348991del GRCh38
NC_000023.10:g.100603975_100603979del , CM000685.1:g.100603975_100603979del GRCh37
NC_000023.9:g.100490631_100490635del NCBI36
NG_009616.1:g.42242_42246del , LRG_128:g.42242_42246del
NG_011734.1:g.4987_4991del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.3:c.-319_-315del ENSP00000361993.3:n.-319_-315del