Canonical Allele Identifier: CA797777165
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs558459621
gnomAD v4: 4-68646638-T-TTTA
MyVariant Identifiers: chr4:g.69512356_69512357insTTA (hg19) chr4:g.68646638_68646639insTTA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646638_68646639insTTA , CM000666.2:g.68646638_68646639insTTA GRCh38
NC_000004.11:g.69512356_69512357insTTA , CM000666.1:g.69512356_69512357insTTA GRCh37
NC_000004.10:g.69194951_69194952insTTA NCBI36
NG_052676.1:g.29138_29139insTAA

Transcript Alleles

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