Canonical Allele Identifier: CA324169063
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs908502849

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37768032C>T , CM000684.2:g.37768032C>T GRCh38
NC_000022.10:g.38164039C>T , CM000684.1:g.38164039C>T GRCh37
NC_000022.9:g.36493985C>T NCBI36
NG_012857.1:g.76045C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.6473-42C>T MANE Select ENSP00000496394.1:n.6473-42C>T
ENST00000344404.10:c.*5956-42C>T ENSP00000340312.6:n.*5956-42C>T
ENST00000403663.6:c.1334-42C>T ENSP00000386026.2:n.1334-42C>T
ENST00000406386.7:c.6473-42C>T ENSP00000384312.3:n.6473-42C>T
NM_001039141.2:c.6473-42C>T NP_001034230.1:n.6473-42C>T
NM_007032.5:c.1334-42C>T NP_008963.3:n.1334-42C>T
NM_001039141.3:c.6473-42C>T MANE Select NP_001034230.1:n.6473-42C>T