Canonical Allele Identifier: CA2680219528
Gene: TRDN HGNC NCBI

Linked Data

gnomAD v4: 6-123218795-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.123218795C>T , CM000668.2:g.123218795C>T GRCh38
NC_000006.11:g.123539940C>T , CM000668.1:g.123539940C>T GRCh37
NC_000006.10:g.123581639C>T NCBI36
NG_030438.1:g.423299G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000334268.9:c.2051-55G>A MANE Select ENSP00000333984.5:n.2051-55G>A
ENST00000334268.8:c.2051-55G>A ENSP00000333984.5:n.2051-55G>A
NM_006073.3:c.2051-55G>A NP_006064.2:n.2051-55G>A
XM_011535382.1:c.1970-55G>A XP_011533684.1:n.1970-55G>A
NM_006073.4:c.2051-55G>A MANE Select NP_006064.2:n.2051-55G>A
Search 100 bp 5'
Search 100 bp 3'