Canonical Allele Identifier: CA766278047

Gene: UGT1A10 UGT1A8 UGT1A9

Linked Data

• dbSNP Id: rs1475250868
• MyVariant Identifiers: chr2:g.234584254C>T (hg19) ; chr2:g.233675608C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233675608C>T , CM000664.2:g.233675608C>T	GRCh38
NC_000002.11:g.234584254C>T , CM000664.1:g.234584254C>T	GRCh37
NC_000002.10:g.234248993C>T	NCBI36
NG_002601.2:g.90865C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000344644.10:c.855+38231C>T (UGT1A10) MANE Select	ENSP00000343838.5:n.855+38231C>T
ENST00000373450.5:c.855+57046C>T (UGT1A8) MANE Select	ENSP00000362549.4:n.855+57046C>T
ENST00000354728.5:c.855+2819C>T (UGT1A9) MANE Select	ENSP00000346768.4:n.855+2819C>T
ENST00000344644.9:c.855+38231C>T (UGT1A10)	ENSP00000343838.5:n.855+38231C>T
ENST00000354728.4:c.855+2819C>T (UGT1A9)	ENSP00000346768.4:n.855+2819C>T
ENST00000373445.1:c.855+38231C>T (UGT1A10)	ENSP00000362544.1:n.855+38231C>T
ENST00000373450.4:c.855+57046C>T (UGT1A8)	ENSP00000362549.4:n.855+57046C>T
NM_019075.2:c.855+38231C>T (UGT1A10)	NP_061948.1:n.855+38231C>T
NM_019076.4:c.855+57046C>T (UGT1A8)	NP_061949.3:n.855+57046C>T
NM_021027.2:c.855+2819C>T (UGT1A9)	NP_066307.1:n.855+2819C>T
NM_021027.3:c.855+2819C>T (UGT1A9) MANE Select	NP_066307.1:n.855+2819C>T
NM_019075.4:c.855+38231C>T (UGT1A10) MANE Select	NP_061948.1:n.855+38231C>T
NM_019076.5:c.855+57046C>T (UGT1A8) MANE Select	NP_061949.3:n.855+57046C>T