Canonical Allele Identifier: CA452054393
Gene: TRDN HGNC NCBI

Linked Data

gnomAD v4: 6-123218661-G-A
MyVariant Identifiers: chr6:g.123539806G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.123218661G>A , CM000668.2:g.123218661G>A GRCh38
NC_000006.11:g.123539806G>A , CM000668.1:g.123539806G>A GRCh37
NC_000006.10:g.123581505G>A NCBI36
NG_030438.1:g.423433C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000334268.9:c.2130C>T MANE Select ENSP00000333984.5:p.Asp710=
ENST00000334268.8:c.2130C>T ENSP00000333984.5:p.Asp710=
NM_006073.3:c.2130C>T NP_006064.2:p.Asp710=
XM_011535382.1:c.2049C>T XP_011533684.1:p.Asp683=
NM_006073.4:c.2130C>T MANE Select NP_006064.2:p.Asp710=
Search 100 bp 5'
Search 100 bp 3'