Canonical Allele Identifier: CA351067074
Gene: UGT1A10 HGNC NCBI
UGT1A8 HGNC NCBI

Linked Data

gnomAD v4: 2-233637327-A-T
MyVariant Identifiers: chr2:g.234545973A>T (hg19) chr2:g.233637327A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233637327A>T , CM000664.2:g.233637327A>T GRCh38
NC_000002.11:g.234545973A>T , CM000664.1:g.234545973A>T GRCh37
NC_000002.10:g.234210712A>T NCBI36
NG_002601.2:g.52584A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344644.10:c.805A>T (UGT1A10) MANE Select ENSP00000343838.5:p.Met269Leu
ENST00000373450.5:c.855+18765A>T (UGT1A8) MANE Select ENSP00000362549.4:n.855+18765A>T
ENST00000344644.9:c.805A>T (UGT1A10) ENSP00000343838.5:p.Met269Leu
ENST00000373445.1:c.805A>T (UGT1A10) ENSP00000362544.1:p.Met269Leu
ENST00000373450.4:c.855+18765A>T (UGT1A8) ENSP00000362549.4:n.855+18765A>T
NM_019075.2:c.805A>T (UGT1A10) NP_061948.1:p.Met269Leu
NM_019076.4:c.855+18765A>T (UGT1A8) NP_061949.3:n.855+18765A>T
NM_019075.4:c.805A>T (UGT1A10) MANE Select NP_061948.1:p.Met269Leu
NM_019076.5:c.855+18765A>T (UGT1A8) MANE Select NP_061949.3:n.855+18765A>T
Search 100 bp 5'
Search 100 bp 3'