Canonical Allele Identifier: CA1135842207
Gene: TIMM8A HGNC NCBI

Linked Data

dbSNP Id: rs1759731517
gnomAD v3: X-101348935-G-A
gnomAD v4: X-101348935-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348935G>A , CM000685.2:g.101348935G>A GRCh38
NC_000023.10:g.100603923G>A , CM000685.1:g.100603923G>A GRCh37
NC_000023.9:g.100490579G>A NCBI36
NG_009616.1:g.42290C>T , LRG_128:g.42290C>T
NG_011734.1:g.5035C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.3:c.-271C>T ENSP00000361993.3:n.-271C>T
NM_004085.3:c.-271C>T NP_004076.1:n.-271C>T
Search 100 bp 5'
Search 100 bp 3'