Canonical Allele Identifier: CA2561691332
Gene: TIMM8A HGNC NCBI

Linked Data

gnomAD v4: X-101348765-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348765G>A , CM000685.2:g.101348765G>A GRCh38
NC_000023.10:g.100603753G>A , CM000685.1:g.100603753G>A GRCh37
NC_000023.9:g.100490409G>A NCBI36
NG_009616.1:g.42460C>T , LRG_128:g.42460C>T
NG_011734.1:g.5205C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.3:c.-101C>T ENSP00000361993.3:n.-101C>T
NM_004085.3:c.-101C>T NP_004076.1:n.-101C>T
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