Canonical Allele Identifier: CA6146675

Gene: TCIRG1

Linked Data

• ClinVar Variation Id: 305782
• ClinVar RCV Id: RCV000358674 ; RCV000456098 ; RCV001517192 ; RCV002278385
• dbSNP Id: rs36027301
• ExAC: 11:67809268 C / T
• gnomAD v2: 11-67809268-C-T
• gnomAD v3: 11-68041801-C-T
• gnomAD v4: 11-68041801-C-T
• MyVariant Identifiers: chr11:g.67809268C>T (hg19) ; chr11:g.68041801C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68041801C>T , CM000673.2:g.68041801C>T	GRCh38
NC_000011.9:g.67809268C>T , CM000673.1:g.67809268C>T	GRCh37
NC_000011.8:g.67565844C>T	NCBI36
NG_007878.1:g.7786C>T , LRG_115:g.7786C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.166C>T	ENSP00000513629.1:p.Arg56Trp
ENST00000698255.1:c.166C>T	ENSP00000513630.1:p.Arg56Trp
ENST00000265686.8:c.166C>T MANE Select	ENSP00000265686.3:p.Arg56Trp
ENST00000265686.7:c.166C>T	ENSP00000265686.3:p.Arg56Trp
ENST00000524598.5:c.124C>T	ENSP00000432846.1:p.Arg42Trp
ENST00000529657.1:c.166C>T	ENSP00000435023.1:p.Arg56Trp
ENST00000533947.1:n.133C>T
ENST00000534673.5:c.166C>T	ENSP00000431174.1:p.Arg56Trp
NM_006019.3:c.166C>T	NP_006010.2:p.Arg56Trp
XM_005273709.2:c.166C>T	XP_005273766.1:p.Arg56Trp
XM_011544726.1:c.166C>T	XP_011543028.1:p.Arg56Trp
XM_011544727.1:c.166C>T	XP_011543029.1:p.Arg56Trp
XM_011544728.1:c.166C>T	XP_011543030.1:p.Arg56Trp
XM_011544729.1:c.166C>T	XP_011543031.1:p.Arg56Trp
XR_949754.1:n.170C>T
NM_001351059.1:c.-1084C>T	NP_001337988.1:n.-1084C>T
XM_024448320.1:c.166C>T	XP_024304088.1:p.Arg56Trp
XM_024448321.1:c.166C>T	XP_024304089.1:p.Arg56Trp
XM_024448322.1:c.166C>T	XP_024304090.1:p.Arg56Trp
XM_024448323.1:c.166C>T	XP_024304091.1:p.Arg56Trp
XM_024448324.1:c.166C>T	XP_024304092.1:p.Arg56Trp
XR_001747721.2:n.290C>T
XR_001747722.1:n.287C>T
XR_001747723.2:n.287C>T
XR_002957115.1:n.288C>T
NM_006019.4:c.166C>T MANE Select	NP_006010.2:p.Arg56Trp
NM_001351059.2:c.-1084C>T	NP_001337988.1:n.-1084C>T