Canonical Allele Identifier: CA643063412
Gene: TIMM8A HGNC NCBI

Linked Data

dbSNP Id: rs1268163416
gnomAD v2: X-100603972-AAAAG-A
gnomAD v3: X-101348984-AAAAG-A
gnomAD v4: X-101348984-AAAAG-A
MyVariant Identifiers: chrX:g.100603973_100603976del (hg19) chrX:g.101348985_101348988del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348989_101348992del , CM000685.2:g.101348989_101348992del GRCh38
NC_000023.10:g.100603977_100603980del , CM000685.1:g.100603977_100603980del GRCh37
NC_000023.9:g.100490633_100490636del NCBI36
NG_009616.1:g.42237_42240del , LRG_128:g.42237_42240del
NG_011734.1:g.4982_4985del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.3:c.-324_-321del ENSP00000361993.3:n.-324_-321del
Search 100 bp 5'
Search 100 bp 3'