Canonical Allele Identifier: CA643063407
Gene: TIMM8A HGNC NCBI

Linked Data

dbSNP Id: rs1197411463
gnomAD v2: X-100603958-GTTAC-G
gnomAD v3: X-101348970-GTTAC-G
gnomAD v4: X-101348970-GTTAC-G
MyVariant Identifiers: chrX:g.100603959_100603962del (hg19) chrX:g.101348971_101348974del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348972_101348975del , CM000685.2:g.101348972_101348975del GRCh38
NC_000023.10:g.100603960_100603963del , CM000685.1:g.100603960_100603963del GRCh37
NC_000023.9:g.100490616_100490619del NCBI36
NG_009616.1:g.42251_42254del , LRG_128:g.42251_42254del
NG_011734.1:g.4996_4999del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.3:c.-310_-307del ENSP00000361993.3:n.-310_-307del
Search 100 bp 5'
Search 100 bp 3'