Canonical Allele Identifier: CA1335897441

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233773302T= , CM000664.2:g.233773302T= GRCh38
NC_000002.11:g.234681948T= , CM000664.1:g.234681948T= GRCh37
NC_000002.10:g.234346687T= NCBI36
NG_002601.2:g.188559T=
NG_033238.1:g.18030T= , LRG_733:g.18030T=
NG_051337.1:g.2641T=

Transcript Alleles

HGVS Amino-acid change
ENST00000344644.9:c.*743T= (UGT1A10) ENSP00000343838.5:n.*743T=
ENST00000373450.4:c.*743T= (UGT1A8) ENSP00000362549.4:n.*743T=
NM_001072.3:c.*743T= (UGT1A6) NP_001063.2:n.*743T=
NM_019075.2:c.*743T= (UGT1A10) NP_061948.1:n.*743T=
NM_021027.2:c.*743T= (UGT1A9) NP_066307.1:n.*743T=