Canonical Allele Identifier: CA2448281615
Gene: TIMM8A HGNC NCBI

Linked Data

dbSNP Id: rs1722336063

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101348914G>C , CM000685.2:g.101348914G>C GRCh38
NC_000023.10:g.100603902G>C , CM000685.1:g.100603902G>C GRCh37
NC_000023.9:g.100490558G>C NCBI36
NG_009616.1:g.42311C>G , LRG_128:g.42311C>G
NG_011734.1:g.5056C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372902.3:c.-250C>G ENSP00000361993.3:n.-250C>G
NM_004085.3:c.-250C>G NP_004076.1:n.-250C>G