Canonical Allele Identifier: CA15394810
Gene: TMCO6 HGNC NCBI
MyVariant.info:
GRCh38 chr5:g.140633722G>A
GRCh37 chr5:g.140013307G>A
gnomAD v2:
5:140013307 G / A
gnomAD v3:
5:140633722 G / A
gnomAD v4:
chr5-140633722-G-A
Joint Max Group AF 0.28337442 (EAS)
Genomes Max Group AF 0.28337442 (EAS)
Exomes Max Group AF 0.13912474 (NFE)
dbSNP:
5744455
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140633722G>A , CM000667.2:g.140633722G>A GRCh38
NC_000005.9:g.140013307G>A , CM000667.1:g.140013307G>A GRCh37
NC_000005.8:g.139993491G>A NCBI36
NG_023178.1:g.4980C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011537665.1:c.-129-7943G>A XP_011535967.1:n.-129-7943G>A
XM_011537665.2:c.-129-7943G>A XP_011535967.1:n.-129-7943G>A
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