Canonical Allele Identifier: CA552177721
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1444305732
gnomAD v2: 4-69512345-T-C
MyVariant Identifiers: chr4:g.69512345T>C (hg19) chr4:g.68646627T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646627T>C , CM000666.2:g.68646627T>C GRCh38
NC_000004.11:g.69512345T>C , CM000666.1:g.69512345T>C GRCh37
NC_000004.10:g.69194940T>C NCBI36
NG_052676.1:g.29150A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*477A>G MANE Select ENSP00000341045.5:n.*477A>G
ENST00000616841.4:c.1732+338A>G ENSP00000482004.1:n.1732+338A>G
NM_001076.3:c.*477A>G NP_001067.2:n.*477A>G
NM_001076.4:c.*477A>G MANE Select NP_001067.2:n.*477A>G
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