Canonical Allele Identifier: CA2694293941
Gene: TIMM8A HGNC NCBI

Linked Data

gnomAD v4: X-101348975-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348975T>C , CM000685.2:g.101348975T>C GRCh38
NC_000023.10:g.100603963T>C , CM000685.1:g.100603963T>C GRCh37
NC_000023.9:g.100490619T>C NCBI36
NG_009616.1:g.42250A>G , LRG_128:g.42250A>G
NG_011734.1:g.4995A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.3:c.-311A>G ENSP00000361993.3:n.-311A>G
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