Canonical Allele Identifier: CA11327808

Linked Data

dbSNP Id: rs6744284

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233716651C>T , CM000664.2:g.233716651C>T GRCh38
NC_000002.11:g.234625297C>T , CM000664.1:g.234625297C>T GRCh37
NC_000002.10:g.234290036C>T NCBI36
NG_002601.2:g.131908C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000305139.11:c.861+22786C>T MANE Select ENSP00000303174.6:p.=
ENST00000354728.5:c.855+43862C>T MANE Select ENSP00000346768.4:p.=
ENST00000305139.10:c.861+22786C>T ENSP00000303174.6:p.=
ENST00000344644.9:c.856-50383C>T ENSP00000343838.5:p.=
ENST00000354728.4:c.855+43862C>T ENSP00000346768.4:p.=
ENST00000373414.3:n.867+2793C>T ENSP00000362513.3:p.=
ENST00000373424.5:c.60+22786C>T ENSP00000362523.1:p.=
ENST00000373426.3:n.855+33859C>T ENSP00000362525.3:p.=
ENST00000373445.1:c.856-50383C>T ENSP00000362544.1:p.=
ENST00000373450.4:c.856-50383C>T ENSP00000362549.4:p.=
ENST00000406651.1:c.60+22786C>T ENSP00000386107.1:p.=
ENST00000446481.6:c.60+22786C>T ENSP00000401541.1:p.=
ENST00000478062.2:n.182-12853C>T
ENST00000480628.1:n.186+22786C>T
ENST00000484784.2:n.202-1142C>T ENSP00000419780.2:p.=
NM_001072.3:c.861+22786C>T (UGT1A6) NP_001063.2:p.=
NM_019075.2:c.856-50383C>T (UGT1A10) NP_061948.1:p.=
NM_019076.4:c.856-50383C>T (UGT1A8) NP_061949.3:p.=
NM_019077.2:n.855+33859C>T (UGT1A7) NP_061950.2:p.=
NM_019078.1:n.867+2793C>T (UGT1A5) NP_061951.1:p.=
NM_021027.2:c.855+43862C>T (UGT1A9) NP_066307.1:p.=
NM_205862.1:c.60+22786C>T (UGT1A6) NP_995584.1:p.=
NM_001072.4:c.861+22786C>T (UGT1A6) MANE Select NP_001063.2:p.=
NM_021027.3:c.855+43862C>T (UGT1A9) MANE Select NP_066307.1:p.=
NM_205862.2:c.60+22786C>T (UGT1A6) NP_995584.1:p.=
NM_019075.4:c.856-50383C>T (UGT1A10) NP_061948.1:p.=
NM_019076.5:c.856-50383C>T (UGT1A8) MANE Select NP_061949.3:p.=
NM_019077.3:c.855+33859C>T (UGT1A7) MANE Select NP_061950.2:p.=
NM_019078.2:c.867+2793C>T (UGT1A5) MANE Select NP_061951.1:p.=
NM_205862.3:c.60+22786C>T (UGT1A6) NP_995584.1:p.=