Canonical Allele Identifier: CA2694293905
Gene: TIMM8A HGNC NCBI

Linked Data

gnomAD v4: X-101348918-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348918T>C , CM000685.2:g.101348918T>C GRCh38
NC_000023.10:g.100603906T>C , CM000685.1:g.100603906T>C GRCh37
NC_000023.9:g.100490562T>C NCBI36
NG_009616.1:g.42307A>G , LRG_128:g.42307A>G
NG_011734.1:g.5052A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.3:c.-254A>G ENSP00000361993.3:n.-254A>G
NM_004085.3:c.-254A>G NP_004076.1:n.-254A>G
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