Canonical Allele Identifier: CA2694293908
Gene: TIMM8A HGNC NCBI

Linked Data

gnomAD v4: X-101348919-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348919G>T , CM000685.2:g.101348919G>T GRCh38
NC_000023.10:g.100603907G>T , CM000685.1:g.100603907G>T GRCh37
NC_000023.9:g.100490563G>T NCBI36
NG_009616.1:g.42306C>A , LRG_128:g.42306C>A
NG_011734.1:g.5051C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.3:c.-255C>A ENSP00000361993.3:n.-255C>A
NM_004085.3:c.-255C>A NP_004076.1:n.-255C>A
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