Canonical Allele Identifier: CA1465820940
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1732494015

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647023A>C , CM000666.2:g.68647023A>C GRCh38
NC_000004.11:g.69512741A>C , CM000666.1:g.69512741A>C GRCh37
NC_000004.10:g.69195336A>C NCBI36
NG_052676.1:g.28754T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*81T>G MANE Select ENSP00000341045.5:n.*81T>G
ENST00000338206.5:c.*81T>G ENSP00000341045.5:n.*81T>G
ENST00000616841.4:c.1674T>G ENSP00000482004.1:n.1674T>G
NM_001076.3:c.*81T>G NP_001067.2:n.*81T>G
NM_001076.4:c.*81T>G MANE Select NP_001067.2:n.*81T>G