Canonical Allele Identifier: CA333095798

Gene: TIMM8A

Linked Data

• dbSNP Id: rs946821636
• gnomAD v3: X-101348985-A-G
• gnomAD v4: X-101348985-A-G
• MyVariant Identifiers: chrX:g.101348985A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101348985A>G , CM000685.2:g.101348985A>G	GRCh38
NC_000023.10:g.100603973A>G , CM000685.1:g.100603973A>G	GRCh37
NC_000023.9:g.100490629A>G	NCBI36
NG_009616.1:g.42240T>C , LRG_128:g.42240T>C
NG_011734.1:g.4985T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372902.3:c.-321T>C	ENSP00000361993.3:n.-321T>C