Canonical Allele Identifier: CA639202093

Gene: TRIOBP

Linked Data

• dbSNP Id: rs1347675585
• gnomAD v2: 22-38164040-C-T
• MyVariant Identifiers: chr22:g.38164040C>T (hg19) ; chr22:g.37768033C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.37768033C>T , CM000684.2:g.37768033C>T	GRCh38
NC_000022.10:g.38164040C>T , CM000684.1:g.38164040C>T	GRCh37
NC_000022.9:g.36493986C>T	NCBI36
NG_012857.1:g.76046C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000644935.1:c.6473-41C>T MANE Select	ENSP00000496394.1:n.6473-41C>T
ENST00000344404.10:c.*5956-41C>T	ENSP00000340312.6:n.*5956-41C>T
ENST00000403663.6:c.1334-41C>T	ENSP00000386026.2:n.1334-41C>T
ENST00000406386.7:c.6473-41C>T	ENSP00000384312.3:n.6473-41C>T
NM_001039141.2:c.6473-41C>T	NP_001034230.1:n.6473-41C>T
NM_007032.5:c.1334-41C>T	NP_008963.3:n.1334-41C>T
NM_001039141.3:c.6473-41C>T MANE Select	NP_001034230.1:n.6473-41C>T