Canonical Allele Identifier: CA869301835
Gene: TIMM8A HGNC NCBI

Linked Data

dbSNP Id: rs1364944069
MyVariant Identifiers: chrX:g.101348743A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348743A>G , CM000685.2:g.101348743A>G GRCh38
NC_000023.10:g.100603731A>G , CM000685.1:g.100603731A>G GRCh37
NC_000023.9:g.100490387A>G NCBI36
NG_009616.1:g.42482T>C , LRG_128:g.42482T>C
NG_011734.1:g.5227T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.3:c.-79T>C ENSP00000361993.3:n.-79T>C
ENST00000480575.1:n.7T>C
NM_004085.3:c.-79T>C NP_004076.1:n.-79T>C
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