Canonical Allele Identifier: CA98747441
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs558459621
gnomAD v2: 4-69512356-T-TTA
gnomAD v3: 4-68646638-T-TTA
gnomAD v4: 4-68646638-T-TTA
MyVariant Identifiers: chr4:g.69512356_69512357insTA (hg19) chr4:g.69512357_69512372delinsTAATGGCTTGGATGACAC (hg19) chr4:g.68646638_68646639insTA (hg38) chr4:g.68646639_68646654delinsTAATGGCTTGGATGACAC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646638_68646639insTA , CM000666.2:g.68646638_68646639insTA GRCh38
NC_000004.11:g.69512356_69512357insTA , CM000666.1:g.69512356_69512357insTA GRCh37
NC_000004.10:g.69194951_69194952insTA NCBI36
NG_052676.1:g.29138_29139insTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*465_*466insTA MANE Select ENSP00000341045.5:n.*465_*466insTA
ENST00000338206.5:c.*465_*466insTA ENSP00000341045.5:n.*465_*466insTA
ENST00000616841.4:c.1732+326_1732+327insTA ENSP00000482004.1:n.1732+326_1732+327insTA
NM_001076.3:c.*465_*466insTA NP_001067.2:n.*465_*466insTA
NM_001076.4:c.*465_*466insTA MANE Select NP_001067.2:n.*465_*466insTA
Search 100 bp 5'
Search 100 bp 3'