Canonical Allele Identifier: CA869302008
Gene: TIMM8A HGNC NCBI

Linked Data

dbSNP Id: rs1479412860
MyVariant Identifiers: chrX:g.101348983G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348983G>A , CM000685.2:g.101348983G>A GRCh38
NC_000023.10:g.100603971G>A , CM000685.1:g.100603971G>A GRCh37
NC_000023.9:g.100490627G>A NCBI36
NG_009616.1:g.42242C>T , LRG_128:g.42242C>T
NG_011734.1:g.4987C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.3:c.-319C>T ENSP00000361993.3:n.-319C>T
Search 100 bp 5'
Search 100 bp 3'