Canonical Allele Identifier: CA679546812

Gene: TCIRG1

Linked Data

• dbSNP Id: rs1288919138
• gnomAD v3: 11-68039681-G-A
• gnomAD v4: 11-68039681-G-A
• MyVariant Identifiers: chr11:g.67807148G>A (hg19) ; chr11:g.68039681G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68039681G>A , CM000673.2:g.68039681G>A	GRCh38
NC_000011.9:g.67807148G>A , CM000673.1:g.67807148G>A	GRCh37
NC_000011.8:g.67563724G>A	NCBI36
NG_007878.1:g.5666G>A , LRG_115:g.5666G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000698254.1:c.-5+562G>A	ENSP00000513629.1:n.-5+562G>A
ENST00000698255.1:c.-5+562G>A	ENSP00000513630.1:n.-5+562G>A
ENST00000265686.8:c.-5+562G>A MANE Select	ENSP00000265686.3:n.-5+562G>A
ENST00000265686.7:c.-5+562G>A	ENSP00000265686.3:n.-5+562G>A
ENST00000524598.5:c.-5+562G>A	ENSP00000432846.1:n.-5+562G>A
ENST00000529657.1:c.-175-111G>A	ENSP00000435023.1:n.-175-111G>A
ENST00000533947.1:n.5+562G>A
ENST00000534673.5:c.-5+562G>A	ENSP00000431174.1:n.-5+562G>A
NM_006019.3:c.-5+562G>A	NP_006010.2:n.-5+562G>A
XM_005273709.2:c.-175-111G>A	XP_005273766.1:n.-175-111G>A
NM_001351059.1:c.-1254+562G>A	NP_001337988.1:n.-1254+562G>A
XM_024448320.1:c.-5+562G>A	XP_024304088.1:n.-5+562G>A
XM_024448321.1:c.-175-111G>A	XP_024304089.1:n.-175-111G>A
XM_024448323.1:c.-5+562G>A	XP_024304091.1:n.-5+562G>A
XM_024448324.1:c.-5+562G>A	XP_024304092.1:n.-5+562G>A
XR_001747721.2:n.120+562G>A
XR_001747722.1:n.117+562G>A
XR_001747723.2:n.117+562G>A
XR_002957115.1:n.118+562G>A
NM_006019.4:c.-5+562G>A MANE Select	NP_006010.2:n.-5+562G>A
NM_001351059.2:c.-1254+562G>A	NP_001337988.1:n.-1254+562G>A