Canonical Allele Identifier: CA869301908
Gene: TIMM8A HGNC NCBI

Linked Data

dbSNP Id: rs1381214256
gnomAD v3: X-101348833-G-C
gnomAD v4: X-101348833-G-C
MyVariant Identifiers: chrX:g.101348833G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348833G>C , CM000685.2:g.101348833G>C GRCh38
NC_000023.10:g.100603821G>C , CM000685.1:g.100603821G>C GRCh37
NC_000023.9:g.100490477G>C NCBI36
NG_009616.1:g.42392C>G , LRG_128:g.42392C>G
NG_011734.1:g.5137C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.3:c.-169C>G ENSP00000361993.3:n.-169C>G
NM_004085.3:c.-169C>G NP_004076.1:n.-169C>G
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