Canonical Allele Identifier: CA12534068
Gene: TOMM7 HGNC NCBI
MyVariant.info:
GRCh38 chr7:g.22812893C>T
GRCh37 chr7:g.22852512C>T
gnomAD v2:
7:22852512 C / T
gnomAD v3:
7:22812893 C / T
gnomAD v4:
chr7-22812893-C-T
Joint Max Group AF 0.6207476 (EAS)
Genomes Max Group AF 0.61726815 (EAS)
Exomes Max Group AF 0.61774925 (EAS)
dbSNP:
2240727
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22812893C>T , CM000669.2:g.22812893C>T GRCh38
NC_000007.13:g.22852512C>T , CM000669.1:g.22852512C>T GRCh37
NC_000007.12:g.22819037C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000358435.8:c.*277G>A ENSP00000351214.4:n.*277G>A
ENST00000463284.2:n.466G>A
NM_019059.3:c.*277G>A NP_061932.1:n.*277G>A
NM_019059.4:c.*277G>A NP_061932.1:n.*277G>A
Search 100 bp 5'
Search 100 bp 3'