Canonical Allele Identifier: CA869301999
Gene: TIMM8A HGNC NCBI

Linked Data

dbSNP Id: rs1425841235
gnomAD v4: X-101348954-G-C
MyVariant Identifiers: chrX:g.101348954G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348954G>C , CM000685.2:g.101348954G>C GRCh38
NC_000023.10:g.100603942G>C , CM000685.1:g.100603942G>C GRCh37
NC_000023.9:g.100490598G>C NCBI36
NG_009616.1:g.42271C>G , LRG_128:g.42271C>G
NG_011734.1:g.5016C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.3:c.-290C>G ENSP00000361993.3:n.-290C>G
NM_004085.3:c.-290C>G NP_004076.1:n.-290C>G
Search 100 bp 5'
Search 100 bp 3'