Canonical Allele Identifier: CA3983859
Gene: TRDN HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.123274674A>T
GRCh37 chr6:g.123595819A>T
gnomAD v2:
6:123595819 A / T
gnomAD v3:
6:123274674 A / T
gnomAD v4:
chr6-123274674-A-T
Joint Max Group AF 0.00005975 (NFE)
Genomes Max Group AF 0.00001972 (NFE)
Exomes Max Group AF 0.00005991 (NFE)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.123274674A>T , CM000668.2:g.123274674A>T GRCh38
NC_000006.11:g.123595819A>T , CM000668.1:g.123595819A>T GRCh37
NC_000006.10:g.123637518A>T NCBI36
NG_030438.1:g.367420T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000334268.9:c.1568-4T>A MANE Select ENSP00000333984.5:n.1568-4T>A
ENST00000334268.8:c.1568-4T>A ENSP00000333984.5:n.1568-4T>A
NM_006073.3:c.1568-4T>A NP_006064.2:n.1568-4T>A
XM_011535382.1:c.1514-4T>A XP_011533684.1:n.1514-4T>A
NM_006073.4:c.1568-4T>A MANE Select NP_006064.2:n.1568-4T>A
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