Canonical Allele Identifier: CA869301972
Gene: TIMM8A HGNC NCBI

Linked Data

dbSNP Id: rs1407495897
gnomAD v3: X-101348931-C-T
gnomAD v4: X-101348931-C-T
MyVariant Identifiers: chrX:g.101348931C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348931C>T , CM000685.2:g.101348931C>T GRCh38
NC_000023.10:g.100603919C>T , CM000685.1:g.100603919C>T GRCh37
NC_000023.9:g.100490575C>T NCBI36
NG_009616.1:g.42294G>A , LRG_128:g.42294G>A
NG_011734.1:g.5039G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.3:c.-267G>A ENSP00000361993.3:n.-267G>A
NM_004085.3:c.-267G>A NP_004076.1:n.-267G>A
Search 100 bp 5'
Search 100 bp 3'