Canonical Allele Identifier: CA365564712
Gene: TRDN HGNC NCBI

Linked Data

dbSNP Id: rs1775030382
MyVariant Identifiers: chr6:g.123539866C>A (hg19) chr6:g.123218721C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.123218721C>A , CM000668.2:g.123218721C>A GRCh38
NC_000006.11:g.123539866C>A , CM000668.1:g.123539866C>A GRCh37
NC_000006.10:g.123581565C>A NCBI36
NG_030438.1:g.423373G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000334268.9:c.2070G>T MANE Select ENSP00000333984.5:p.Gln690His
ENST00000334268.8:c.2070G>T ENSP00000333984.5:p.Gln690His
NM_006073.3:c.2070G>T NP_006064.2:p.Gln690His
XM_011535382.1:c.1989G>T XP_011533684.1:p.Gln663His
NM_006073.4:c.2070G>T MANE Select NP_006064.2:p.Gln690His
Search 100 bp 5'
Search 100 bp 3'