Canonical Allele Identifier: CA357086762
Gene: UGT2B15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670377A>C , CM000666.2:g.68670377A>C GRCh38
NC_000004.11:g.69536095A>C , CM000666.1:g.69536095A>C GRCh37
NC_000004.10:g.69218690A>C NCBI36
NG_052676.1:g.5400T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000338206.6:c.242T>G MANE Select ENSP00000341045.5:p.Leu81Ter
ENST00000338206.5:c.242T>G ENSP00000341045.5:p.Leu81Ter
ENST00000616841.4:c.242T>G ENSP00000482004.1:p.Leu81Ter
NM_001076.3:c.242T>G NP_001067.2:p.Leu81Ter
NM_001076.4:c.242T>G MANE Select NP_001067.2:p.Leu81Ter