Canonical Allele Identifier: CA11327805
Gene: UGT1A10 HGNC NCBI
UGT1A8 HGNC NCBI

Linked Data

dbSNP Id: rs10929251

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233637583A>G , CM000664.2:g.233637583A>G GRCh38
NC_000002.11:g.234546229A>G , CM000664.1:g.234546229A>G GRCh37
NC_000002.10:g.234210968A>G NCBI36
NG_002601.2:g.52840A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000344644.9:c.855+206A>G ENSP00000343838.5:p.=
ENST00000373445.1:c.855+206A>G ENSP00000362544.1:p.=
ENST00000373450.4:c.855+19021A>G ENSP00000362549.4:p.=
NM_019075.2:c.855+206A>G (UGT1A10) NP_061948.1:p.=
NM_019076.4:c.855+19021A>G (UGT1A8) NP_061949.3:p.=
NM_019075.4:c.855+206A>G (UGT1A10) NP_061948.1:p.=
NM_019076.5:c.855+19021A>G (UGT1A8) MANE Select NP_061949.3:p.=