Canonical Allele Identifier: CA2448281622
Gene: TIMM8A HGNC NCBI

Linked Data

dbSNP Id: rs1926163536
gnomAD v4: X-101348932-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348932G>T , CM000685.2:g.101348932G>T GRCh38
NC_000023.10:g.100603920G>T , CM000685.1:g.100603920G>T GRCh37
NC_000023.9:g.100490576G>T NCBI36
NG_009616.1:g.42293C>A , LRG_128:g.42293C>A
NG_011734.1:g.5038C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.3:c.-268C>A ENSP00000361993.3:n.-268C>A
NM_004085.3:c.-268C>A NP_004076.1:n.-268C>A
Search 100 bp 5'
Search 100 bp 3'