Canonical Allele Identifier: CA2448281642
Gene: TIMM8A HGNC NCBI

Linked Data

dbSNP Id: rs1926165533

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348979A>G , CM000685.2:g.101348979A>G GRCh38
NC_000023.10:g.100603967A>G , CM000685.1:g.100603967A>G GRCh37
NC_000023.9:g.100490623A>G NCBI36
NG_009616.1:g.42246T>C , LRG_128:g.42246T>C
NG_011734.1:g.4991T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.3:c.-315T>C ENSP00000361993.3:n.-315T>C