Canonical Allele Identifier: CA381584856
Gene: TCIRG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1988317
ClinVar RCV Id: RCV002790385
dbSNP Id: rs1366709820
gnomAD v2: 11-67816351-G-A
gnomAD v3: 11-68048884-G-A
gnomAD v4: 11-68048884-G-A
MyVariant Identifiers: chr11:g.67816351G>A (hg19) chr11:g.68048884G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68048884G>A , CM000673.2:g.68048884G>A GRCh38
NC_000011.9:g.67816351G>A , CM000673.1:g.67816351G>A GRCh37
NC_000011.8:g.67572927G>A NCBI36
NG_007878.1:g.14869G>A , LRG_115:g.14869G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000530449.2:n.185G>A
ENST00000698254.1:c.1089G>A ENSP00000513629.1:p.Trp363Ter
ENST00000698255.1:c.1509G>A ENSP00000513630.1:p.Trp503Ter
ENST00000698256.1:c.1026G>A
ENST00000698257.1:n.978G>A
ENST00000698258.1:n.695G>A
ENST00000698259.1:n.461G>A
ENST00000265686.8:c.1560G>A MANE Select ENSP00000265686.3:p.Trp520Ter
ENST00000265686.7:c.1560G>A ENSP00000265686.3:p.Trp520Ter
ENST00000525724.5:n.872G>A
ENST00000528981.5:c.712G>A
ENST00000532635.5:c.912G>A ENSP00000434407.1:p.Trp304Ter
ENST00000533005.5:n.673G>A
NM_006019.3:c.1560G>A NP_006010.2:p.Trp520Ter
NM_006053.3:c.912G>A NP_006044.1:p.Trp304Ter
XM_005273709.2:c.1560G>A XP_005273766.1:p.Trp520Ter
XM_011544726.1:c.1560G>A XP_011543028.1:p.Trp520Ter
XM_011544727.1:c.1560G>A XP_011543029.1:p.Trp520Ter
XM_011544728.1:c.1560G>A XP_011543030.1:p.Trp520Ter
XR_949754.1:n.1564G>A
NM_001351059.1:c.666G>A NP_001337988.1:p.Trp222Ter
XM_024448320.1:c.1653G>A XP_024304088.1:p.Trp551Ter
XM_024448321.1:c.1653G>A XP_024304089.1:p.Trp551Ter
XM_024448322.1:c.1653G>A XP_024304090.1:p.Trp551Ter
XM_024448323.1:c.1653G>A XP_024304091.1:p.Trp551Ter
XM_024448324.1:c.1653G>A XP_024304092.1:p.Trp551Ter
XR_001747721.2:n.1684G>A
XR_001747722.1:n.1697G>A
XR_001747723.2:n.1697G>A
XR_002957115.1:n.1775G>A
NM_006019.4:c.1560G>A MANE Select NP_006010.2:p.Trp520Ter
NM_001351059.2:c.666G>A NP_001337988.1:p.Trp222Ter
NM_006053.4:c.912G>A NP_006044.1:p.Trp304Ter
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