Canonical Allele Identifier: CA2448281536
Gene: TIMM8A HGNC NCBI

Linked Data

dbSNP Id: rs1926155892
gnomAD v4: X-101348751-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348751C>T , CM000685.2:g.101348751C>T GRCh38
NC_000023.10:g.100603739C>T , CM000685.1:g.100603739C>T GRCh37
NC_000023.9:g.100490395C>T NCBI36
NG_009616.1:g.42474G>A , LRG_128:g.42474G>A
NG_011734.1:g.5219G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.3:c.-87G>A ENSP00000361993.3:n.-87G>A
NM_004085.3:c.-87G>A NP_004076.1:n.-87G>A
Search 100 bp 5'
Search 100 bp 3'