Canonical Allele Identifier: CA679554734
Gene: TCIRG1 HGNC NCBI

Linked Data

dbSNP Id: rs1334912925

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68048033T>G , CM000673.2:g.68048033T>G GRCh38
NC_000011.9:g.67815500T>G , CM000673.1:g.67815500T>G GRCh37
NC_000011.8:g.67572076T>G NCBI36
NG_007878.1:g.14018T>G , LRG_115:g.14018T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000530449.2:n.179+61T>G
ENST00000698254.1:c.1083+61T>G ENSP00000513629.1:n.1083+61T>G
ENST00000698255.1:c.1503+61T>G ENSP00000513630.1:n.1503+61T>G
ENST00000698256.1:c.1020+61T>G
ENST00000698257.1:n.972+61T>G
ENST00000698258.1:n.689+61T>G
ENST00000698259.1:n.455+61T>G
ENST00000265686.8:c.1554+61T>G MANE Select ENSP00000265686.3:n.1554+61T>G
ENST00000265686.7:c.1554+61T>G ENSP00000265686.3:n.1554+61T>G
ENST00000525516.1:n.409T>G
ENST00000525724.5:n.866+61T>G
ENST00000528981.5:c.706+61T>G
ENST00000532635.5:c.906+61T>G ENSP00000434407.1:n.906+61T>G
ENST00000533005.5:n.667+61T>G
NM_006019.3:c.1554+61T>G NP_006010.2:n.1554+61T>G
NM_006053.3:c.906+61T>G NP_006044.1:n.906+61T>G
XM_005273709.2:c.1554+61T>G XP_005273766.1:n.1554+61T>G
XM_011544726.1:c.1554+61T>G XP_011543028.1:n.1554+61T>G
XM_011544727.1:c.1554+61T>G XP_011543029.1:n.1554+61T>G
XM_011544728.1:c.1554+61T>G XP_011543030.1:n.1554+61T>G
XR_949754.1:n.1558+61T>G
NM_001351059.1:c.660+61T>G NP_001337988.1:n.660+61T>G
XM_024448320.1:c.1647+61T>G XP_024304088.1:n.1647+61T>G
XM_024448321.1:c.1647+61T>G XP_024304089.1:n.1647+61T>G
XM_024448322.1:c.1647+61T>G XP_024304090.1:n.1647+61T>G
XM_024448323.1:c.1647+61T>G XP_024304091.1:n.1647+61T>G
XM_024448324.1:c.1647+61T>G XP_024304092.1:n.1647+61T>G
XR_001747721.2:n.1678+61T>G
XR_001747722.1:n.1691+61T>G
XR_001747723.2:n.1691+61T>G
XR_002957115.1:n.1769+61T>G
NM_006019.4:c.1554+61T>G MANE Select NP_006010.2:n.1554+61T>G
NM_001351059.2:c.660+61T>G NP_001337988.1:n.660+61T>G
NM_006053.4:c.906+61T>G NP_006044.1:n.906+61T>G