Canonical Allele Identifier: CA333095776
Gene: TIMM8A HGNC NCBI

Linked Data

dbSNP Id: rs201304719
gnomAD v4: X-101348816-T-C
MyVariant Identifiers: chrX:g.100603804T>C (hg19) chrX:g.101348816T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348816T>C , CM000685.2:g.101348816T>C GRCh38
NC_000023.10:g.100603804T>C , CM000685.1:g.100603804T>C GRCh37
NC_000023.9:g.100490460T>C NCBI36
NG_009616.1:g.42409A>G , LRG_128:g.42409A>G
NG_011734.1:g.5154A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.3:c.-152A>G ENSP00000361993.3:n.-152A>G
NM_004085.3:c.-152A>G NP_004076.1:n.-152A>G
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