Canonical Allele Identifier: CA1063752700
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v3: 4-68646764-A-ATTTTTTTT
gnomAD v4: 4-68646764-A-ATTTTTTTT
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646764_68646765insTTTTTTTT , CM000666.2:g.68646764_68646765insTTTTTTTT GRCh38
NC_000004.11:g.69512482_69512483insTTTTTTTT , CM000666.1:g.69512482_69512483insTTTTTTTT GRCh37
NC_000004.10:g.69195077_69195078insTTTTTTTT NCBI36
NG_052676.1:g.29012_29013insAAAAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*339_*340insAAAAAAAA MANE Select ENSP00000341045.5:n.*339_*340insAAAAAAAA
ENST00000338206.5:c.*339_*340insAAAAAAAA ENSP00000341045.5:n.*339_*340insAAAAAAAA
ENST00000616841.4:c.1732+200_1732+201insAAAAAAAA ENSP00000482004.1:n.1732+200_1732+201insAAAAAAAA
NM_001076.3:c.*339_*340insAAAAAAAA NP_001067.2:n.*339_*340insAAAAAAAA
NM_001076.4:c.*339_*340insAAAAAAAA MANE Select NP_001067.2:n.*339_*340insAAAAAAAA
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