Canonical Allele Identifier: CA1335843989
Gene: UGT1A10 HGNC NCBI
UGT1A8 HGNC NCBI

Linked Data

dbSNP Id: rs922680959
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233656555G>A , CM000664.2:g.233656555G>A GRCh38
NC_000002.11:g.234565201G>A , CM000664.1:g.234565201G>A GRCh37
NC_000002.10:g.234229940G>A NCBI36
NG_002601.2:g.71812G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344644.10:c.855+19178G>A (UGT1A10) MANE Select ENSP00000343838.5:n.855+19178G>A
ENST00000373450.5:c.855+37993G>A (UGT1A8) MANE Select ENSP00000362549.4:n.855+37993G>A
ENST00000344644.9:c.855+19178G>A (UGT1A10) ENSP00000343838.5:n.855+19178G>A
ENST00000373445.1:c.855+19178G>A (UGT1A10) ENSP00000362544.1:n.855+19178G>A
ENST00000373450.4:c.855+37993G>A (UGT1A8) ENSP00000362549.4:n.855+37993G>A
NM_019075.2:c.855+19178G>A (UGT1A10) NP_061948.1:n.855+19178G>A
NM_019076.4:c.855+37993G>A (UGT1A8) NP_061949.3:n.855+37993G>A
NM_019075.4:c.855+19178G>A (UGT1A10) MANE Select NP_061948.1:n.855+19178G>A
NM_019076.5:c.855+37993G>A (UGT1A8) MANE Select NP_061949.3:n.855+37993G>A
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