Canonical Allele Identifier: CA869301847
Gene: TIMM8A HGNC NCBI

Linked Data

dbSNP Id: rs1444158196
MyVariant Identifiers: chrX:g.101348787A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348787A>G , CM000685.2:g.101348787A>G GRCh38
NC_000023.10:g.100603775A>G , CM000685.1:g.100603775A>G GRCh37
NC_000023.9:g.100490431A>G NCBI36
NG_009616.1:g.42438T>C , LRG_128:g.42438T>C
NG_011734.1:g.5183T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.3:c.-123T>C ENSP00000361993.3:n.-123T>C
NM_004085.3:c.-123T>C NP_004076.1:n.-123T>C