Canonical Allele Identifier: CA3983606
Gene: TRDN HGNC NCBI

Linked Data

dbSNP Id: rs761962307
ExAC: 6:123539878 G / T
gnomAD v2: 6-123539878-G-T
gnomAD v4: 6-123218733-G-T
MyVariant Identifiers: chr6:g.123539878G>T (hg19) chr6:g.123218733G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.123218733G>T , CM000668.2:g.123218733G>T GRCh38
NC_000006.11:g.123539878G>T , CM000668.1:g.123539878G>T GRCh37
NC_000006.10:g.123581577G>T NCBI36
NG_030438.1:g.423361C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000334268.9:c.2058C>A MANE Select ENSP00000333984.5:p.Ile686=
ENST00000334268.8:c.2058C>A ENSP00000333984.5:p.Ile686=
NM_006073.3:c.2058C>A NP_006064.2:p.Ile686=
XM_011535382.1:c.1977C>A XP_011533684.1:p.Ile659=
NM_006073.4:c.2058C>A MANE Select NP_006064.2:p.Ile686=
Search 100 bp 5'
Search 100 bp 3'