Canonical Allele Identifier: CA2588036552
Gene: TIMM44 HGNC NCBI

Linked Data

gnomAD v4: 19-7943673-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7943673C>G , CM000681.2:g.7943673C>G GRCh38
NC_000019.9:g.8008558C>G , CM000681.1:g.8008558C>G GRCh37
NC_000019.8:g.7914558C>G NCBI36
NG_051180.1:g.5151G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000270538.7:c.-22G>C ENSP00000270538.2:n.-22G>C
NM_006351.3:c.-22G>C NP_006342.2:n.-22G>C