Canonical Allele Identifier: CA869301987

Gene: TIMM8A

Linked Data

• dbSNP Id: rs1167563853
• gnomAD v3: X-101348941-A-G
• gnomAD v4: X-101348941-A-G
• MyVariant Identifiers: chrX:g.101348941A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.101348941A>G , CM000685.2:g.101348941A>G	GRCh38
NC_000023.10:g.100603929A>G , CM000685.1:g.100603929A>G	GRCh37
NC_000023.9:g.100490585A>G	NCBI36
NG_009616.1:g.42284T>C , LRG_128:g.42284T>C
NG_011734.1:g.5029T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372902.3:c.-277T>C	ENSP00000361993.3:n.-277T>C
NM_004085.3:c.-277T>C	NP_004076.1:n.-277T>C