Canonical Allele Identifier: CA11945531
Gene: TMCO6 HGNC NCBI
COSMIC:
COSN20411467 (not active)
MyVariant.info:
GRCh38 chr5:g.140634792C>T
GRCh37 chr5:g.140014377C>T
gnomAD v2:
5:140014377 C / T
gnomAD v3:
5:140634792 C / T
gnomAD v4:
chr5-140634792-C-T
Joint Max Group AF 0.76545747 (AFR)
Genomes Max Group AF 0.76545747 (AFR)
dbSNP:
2915863
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140634792C>T , CM000667.2:g.140634792C>T GRCh38
NC_000005.9:g.140014377C>T , CM000667.1:g.140014377C>T GRCh37
NC_000005.8:g.139994561C>T NCBI36
NG_023178.1:g.3910G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011537665.1:c.-129-6873C>T XP_011535967.1:n.-129-6873C>T
XM_011537665.2:c.-129-6873C>T XP_011535967.1:n.-129-6873C>T
Search 100 bp 5'
Search 100 bp 3'