Canonical Allele Identifier: CA6147056

Gene: TCIRG1

Linked Data

• ClinVar Variation Id: 1110964
• ClinVar RCV Id: RCV001437394
• dbSNP Id: rs369478607
• ExAC: 11:67815048 C / T
• gnomAD v2: 11-67815048-C-T
• gnomAD v3: 11-68047581-C-T
• gnomAD v4: 11-68047581-C-T
• MyVariant Identifiers: chr11:g.67815048C>T (hg19) ; chr11:g.68047581C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047581C>T , CM000673.2:g.68047581C>T	GRCh38
NC_000011.9:g.67815048C>T , CM000673.1:g.67815048C>T	GRCh37
NC_000011.8:g.67571624C>T	NCBI36
NG_007878.1:g.13566C>T , LRG_115:g.13566C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.834+9C>T	ENSP00000513629.1:n.834+9C>T
ENST00000698255.1:c.1254+9C>T	ENSP00000513630.1:n.1254+9C>T
ENST00000698256.1:c.771+9C>T
ENST00000698257.1:n.723+9C>T
ENST00000698258.1:n.298C>T
ENST00000698259.1:n.129+9C>T
ENST00000265686.8:c.1305+9C>T MANE Select	ENSP00000265686.3:n.1305+9C>T
ENST00000265686.7:c.1305+9C>T	ENSP00000265686.3:n.1305+9C>T
ENST00000525516.1:n.99+9C>T
ENST00000525724.5:n.617+9C>T
ENST00000528981.5:c.457+9C>T
ENST00000529364.1:c.716+9C>T
ENST00000532635.5:c.657+9C>T	ENSP00000434407.1:n.657+9C>T
ENST00000533005.5:n.341+9C>T
NM_006019.3:c.1305+9C>T	NP_006010.2:n.1305+9C>T
NM_006053.3:c.657+9C>T	NP_006044.1:n.657+9C>T
XM_005273709.2:c.1305+9C>T	XP_005273766.1:n.1305+9C>T
XM_011544726.1:c.1305+9C>T	XP_011543028.1:n.1305+9C>T
XM_011544727.1:c.1305+9C>T	XP_011543029.1:n.1305+9C>T
XM_011544728.1:c.1305+9C>T	XP_011543030.1:n.1305+9C>T
XM_011544729.1:c.1321+9C>T	XP_011543031.1:n.1321+9C>T
XR_949754.1:n.1309+9C>T
NM_001351059.1:c.411+9C>T	NP_001337988.1:n.411+9C>T
XM_024448320.1:c.1321+9C>T	XP_024304088.1:n.1321+9C>T
XM_024448321.1:c.1321+9C>T	XP_024304089.1:n.1321+9C>T
XM_024448322.1:c.1321+9C>T	XP_024304090.1:n.1321+9C>T
XM_024448323.1:c.1321+9C>T	XP_024304091.1:n.1321+9C>T
XM_024448324.1:c.1321+9C>T	XP_024304092.1:n.1321+9C>T
XR_001747721.2:n.1429+9C>T
XR_001747722.1:n.1442+9C>T
XR_001747723.2:n.1442+9C>T
XR_002957115.1:n.1443+9C>T
NM_006019.4:c.1305+9C>T MANE Select	NP_006010.2:n.1305+9C>T
NM_001351059.2:c.411+9C>T	NP_001337988.1:n.411+9C>T
NM_006053.4:c.657+9C>T	NP_006044.1:n.657+9C>T