Canonical Allele Identifier: CA365564775
Gene: TRDN HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.123539875A>C (hg19) chr6:g.123218730A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.123218730A>C , CM000668.2:g.123218730A>C GRCh38
NC_000006.11:g.123539875A>C , CM000668.1:g.123539875A>C GRCh37
NC_000006.10:g.123581574A>C NCBI36
NG_030438.1:g.423364T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000334268.9:c.2061T>G MANE Select ENSP00000333984.5:p.Ser687Arg
ENST00000334268.8:c.2061T>G ENSP00000333984.5:p.Ser687Arg
NM_006073.3:c.2061T>G NP_006064.2:p.Ser687Arg
XM_011535382.1:c.1980T>G XP_011533684.1:p.Ser660Arg
NM_006073.4:c.2061T>G MANE Select NP_006064.2:p.Ser687Arg
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