Canonical Allele Identifier: CA1465820923
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1732492934

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646996A>C , CM000666.2:g.68646996A>C GRCh38
NC_000004.11:g.69512714A>C , CM000666.1:g.69512714A>C GRCh37
NC_000004.10:g.69195309A>C NCBI36
NG_052676.1:g.28781T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*108T>G MANE Select ENSP00000341045.5:n.*108T>G
ENST00000338206.5:c.*108T>G ENSP00000341045.5:n.*108T>G
ENST00000616841.4:c.1701T>G ENSP00000482004.1:n.1701T>G
NM_001076.3:c.*108T>G NP_001067.2:n.*108T>G
NM_001076.4:c.*108T>G MANE Select NP_001067.2:n.*108T>G