Canonical Allele Identifier: CA2694293752
Gene: TIMM8A HGNC NCBI

Linked Data

gnomAD v4: X-101348744-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348744G>A , CM000685.2:g.101348744G>A GRCh38
NC_000023.10:g.100603732G>A , CM000685.1:g.100603732G>A GRCh37
NC_000023.9:g.100490388G>A NCBI36
NG_009616.1:g.42481C>T , LRG_128:g.42481C>T
NG_011734.1:g.5226C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.3:c.-80C>T ENSP00000361993.3:n.-80C>T
ENST00000480575.1:n.6C>T
NM_004085.3:c.-80C>T NP_004076.1:n.-80C>T
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