Canonical Allele Identifier: CA570326870
Gene: TRDN HGNC NCBI

Linked Data

dbSNP Id: rs1272308728
gnomAD v2: 6-123539932-C-A
gnomAD v3: 6-123218787-C-A
gnomAD v4: 6-123218787-C-A
MyVariant Identifiers: chr6:g.123539932C>A (hg19) chr6:g.123218787C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.123218787C>A , CM000668.2:g.123218787C>A GRCh38
NC_000006.11:g.123539932C>A , CM000668.1:g.123539932C>A GRCh37
NC_000006.10:g.123581631C>A NCBI36
NG_030438.1:g.423307G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000334268.9:c.2051-47G>T MANE Select ENSP00000333984.5:n.2051-47G>T
ENST00000334268.8:c.2051-47G>T ENSP00000333984.5:n.2051-47G>T
NM_006073.3:c.2051-47G>T NP_006064.2:n.2051-47G>T
XM_011535382.1:c.1970-47G>T XP_011533684.1:n.1970-47G>T
NM_006073.4:c.2051-47G>T MANE Select NP_006064.2:n.2051-47G>T
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