Canonical Allele Identifier: CA540055369

Gene: UGT1A10 UGT1A8

Linked Data

• dbSNP Id: rs1350213074
• gnomAD v2: 2-234565122-T-C
• gnomAD v3: 2-233656476-T-C
• gnomAD v4: 2-233656476-T-C
• MyVariant Identifiers: chr2:g.234565122T>C (hg19) ; chr2:g.233656476T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233656476T>C , CM000664.2:g.233656476T>C	GRCh38
NC_000002.11:g.234565122T>C , CM000664.1:g.234565122T>C	GRCh37
NC_000002.10:g.234229861T>C	NCBI36
NG_002601.2:g.71733T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000344644.10:c.855+19099T>C (UGT1A10) MANE Select	ENSP00000343838.5:n.855+19099T>C
ENST00000373450.5:c.855+37914T>C (UGT1A8) MANE Select	ENSP00000362549.4:n.855+37914T>C
ENST00000344644.9:c.855+19099T>C (UGT1A10)	ENSP00000343838.5:n.855+19099T>C
ENST00000373445.1:c.855+19099T>C (UGT1A10)	ENSP00000362544.1:n.855+19099T>C
ENST00000373450.4:c.855+37914T>C (UGT1A8)	ENSP00000362549.4:n.855+37914T>C
NM_019075.2:c.855+19099T>C (UGT1A10)	NP_061948.1:n.855+19099T>C
NM_019076.4:c.855+37914T>C (UGT1A8)	NP_061949.3:n.855+37914T>C
NM_019075.4:c.855+19099T>C (UGT1A10) MANE Select	NP_061948.1:n.855+19099T>C
NM_019076.5:c.855+37914T>C (UGT1A8) MANE Select	NP_061949.3:n.855+37914T>C