Canonical Allele Identifier: CA2321174324
Gene: TIMM44 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7943672T= , CM000681.2:g.7943672T= GRCh38
NC_000019.9:g.8008557T= , CM000681.1:g.8008557T= GRCh37
NC_000019.8:g.7914557T= NCBI36
NG_051180.1:g.5152A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270538.7:c.-21A= ENSP00000270538.2:n.-21A=
NM_006351.3:c.-21A= NP_006342.2:n.-21A=