Canonical Allele Identifier: CA365564698
Gene: TRDN HGNC NCBI

Linked Data

ClinVar Variation Id: 1506821
ClinVar RCV Id: RCV002548110
dbSNP Id: rs2114492427
MyVariant Identifiers: chr6:g.123539864C>G (hg19) chr6:g.123218719C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.123218719C>G , CM000668.2:g.123218719C>G GRCh38
NC_000006.11:g.123539864C>G , CM000668.1:g.123539864C>G GRCh37
NC_000006.10:g.123581563C>G NCBI36
NG_030438.1:g.423375G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000334268.9:c.2072G>C MANE Select ENSP00000333984.5:p.Cys691Ser
ENST00000334268.8:c.2072G>C ENSP00000333984.5:p.Cys691Ser
NM_006073.3:c.2072G>C NP_006064.2:p.Cys691Ser
XM_011535382.1:c.1991G>C XP_011533684.1:p.Cys664Ser
NM_006073.4:c.2072G>C MANE Select NP_006064.2:p.Cys691Ser
Search 100 bp 5'
Search 100 bp 3'