Canonical Allele Identifier: CA6147518
Gene: TCIRG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 283600
dbSNP Id: rs141356870

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68050647C>T , CM000673.2:g.68050647C>T GRCh38
NC_000011.9:g.67818114C>T , CM000673.1:g.67818114C>T GRCh37
NC_000011.8:g.67574690C>T NCBI36
NG_007878.1:g.16632C>T , LRG_115:g.16632C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000530449.2:n.1622C>T
ENST00000698254.1:c.1926C>T ENSP00000513629.1:p.His642=
ENST00000698255.1:c.2346C>T ENSP00000513630.1:p.His782=
ENST00000698257.1:n.1815C>T
ENST00000698258.1:n.1532C>T
ENST00000265686.8:c.2397C>T MANE Select ENSP00000265686.3:p.His799=
ENST00000265686.7:c.2397C>T ENSP00000265686.3:p.His799=
ENST00000525724.5:n.1709C>T
ENST00000530063.1:c.140-94C>T ENSP00000432957.1:n.140-94C>T
ENST00000530449.1:n.525C>T
ENST00000530802.1:n.143-94C>T
ENST00000532635.5:c.1749C>T ENSP00000434407.1:p.His583=
ENST00000533005.5:n.1510C>T
NM_006019.3:c.2397C>T NP_006010.2:p.His799=
NM_006053.3:c.1749C>T NP_006044.1:p.His583=
XM_005273709.2:c.2397C>T XP_005273766.1:p.His799=
XM_011544726.1:c.2397C>T XP_011543028.1:p.His799=
XM_011544727.1:c.2237-94C>T XP_011543029.1:n.2237-94C>T
XR_949754.1:n.2544C>T
NM_001351059.1:c.1503C>T NP_001337988.1:p.His501=
XM_024448320.1:c.2490C>T XP_024304088.1:p.His830=
XM_024448321.1:c.2490C>T XP_024304089.1:p.His830=
XM_024448322.1:c.2490C>T XP_024304090.1:p.His830=
XM_024448323.1:c.2490C>T XP_024304091.1:p.His830=
XR_001747721.2:n.2566C>T
XR_001747722.1:n.2534C>T
XR_001747723.2:n.2579C>T
XR_002957115.1:n.2755C>T
NM_006019.4:c.2397C>T MANE Select NP_006010.2:p.His799=
NM_001351059.2:c.1503C>T NP_001337988.1:p.His501=
NM_006053.4:c.1749C>T NP_006044.1:p.His583=