Canonical Allele Identifier: CA333095779
Gene: TIMM8A HGNC NCBI

Linked Data

dbSNP Id: rs782533809
gnomAD v2: X-100603808-A-G
gnomAD v3: X-101348820-A-G
gnomAD v4: X-101348820-A-G
MyVariant Identifiers: chrX:g.100603808A>G (hg19) chrX:g.101348820A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348820A>G , CM000685.2:g.101348820A>G GRCh38
NC_000023.10:g.100603808A>G , CM000685.1:g.100603808A>G GRCh37
NC_000023.9:g.100490464A>G NCBI36
NG_009616.1:g.42405T>C , LRG_128:g.42405T>C
NG_011734.1:g.5150T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.3:c.-156T>C ENSP00000361993.3:n.-156T>C
NM_004085.3:c.-156T>C NP_004076.1:n.-156T>C
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