Canonical Allele Identifier: CA2581422327
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646788G>C , CM000666.2:g.68646788G>C GRCh38
NC_000004.11:g.69512506G>C , CM000666.1:g.69512506G>C GRCh37
NC_000004.10:g.69195101G>C NCBI36
NG_052676.1:g.28989C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*316C>G MANE Select ENSP00000341045.5:n.*316C>G
ENST00000338206.5:c.*316C>G ENSP00000341045.5:n.*316C>G
ENST00000616841.4:c.1732+177C>G ENSP00000482004.1:n.1732+177C>G
NM_001076.3:c.*316C>G NP_001067.2:n.*316C>G
NM_001076.4:c.*316C>G MANE Select NP_001067.2:n.*316C>G