Canonical Allele Identifier: CA1063752319
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v3: 4-68646628-C-CTT
gnomAD v4: 4-68646628-C-CTT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646637_68646638dup , CM000666.2:g.68646637_68646638dup GRCh38
NC_000004.11:g.69512355_69512356dup , CM000666.1:g.69512355_69512356dup GRCh37
NC_000004.10:g.69194950_69194951dup NCBI36
NG_052676.1:g.29147_29148dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*474_*475dup MANE Select ENSP00000341045.5:n.*474_*475dup
ENST00000616841.4:c.1732+335_1732+336dup ENSP00000482004.1:n.1732+335_1732+336dup
NM_001076.3:c.*474_*475dup NP_001067.2:n.*474_*475dup
NM_001076.4:c.*474_*475dup MANE Select NP_001067.2:n.*474_*475dup
Search 100 bp 5'
Search 100 bp 3'