Canonical Allele Identifier: CA552177726
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1732476710
gnomAD v2: 4-69512356-TATGGCTTGGATGACAC-T
gnomAD v3: 4-68646638-TATGGCTTGGATGACAC-T
gnomAD v4: 4-68646638-TATGGCTTGGATGACAC-T
MyVariant Identifiers: chr4:g.69512357_69512372del (hg19) chr4:g.68646639_68646654del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646639_68646654del , CM000666.2:g.68646639_68646654del GRCh38
NC_000004.11:g.69512357_69512372del , CM000666.1:g.69512357_69512372del GRCh37
NC_000004.10:g.69194952_69194967del NCBI36
NG_052676.1:g.29123_29138del

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*450_*465del MANE Select ENSP00000341045.5:n.*450_*465del
ENST00000338206.5:c.*450_*465del ENSP00000341045.5:n.*450_*465del
ENST00000616841.4:c.1732+311_1732+326del ENSP00000482004.1:n.1732+311_1732+326del
NM_001076.3:c.*450_*465del NP_001067.2:n.*450_*465del
NM_001076.4:c.*450_*465del MANE Select NP_001067.2:n.*450_*465del
Search 100 bp 5'
Search 100 bp 3'