Canonical Allele Identifier: CA884257258
Gene: TIMM44 HGNC NCBI

Linked Data

dbSNP Id: rs1433347647
gnomAD v3: 19-7943680-C-T
gnomAD v4: 19-7943680-C-T
MyVariant Identifiers: chr19:g.8008565C>T (hg19) chr19:g.7943680C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7943680C>T , CM000681.2:g.7943680C>T GRCh38
NC_000019.9:g.8008565C>T , CM000681.1:g.8008565C>T GRCh37
NC_000019.8:g.7914565C>T NCBI36
NG_051180.1:g.5144G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000270538.7:c.-29G>A ENSP00000270538.2:n.-29G>A
NM_006351.3:c.-29G>A NP_006342.2:n.-29G>A
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