Canonical Allele Identifier: CA357083021
Gene: UGT2B15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647164T>G , CM000666.2:g.68647164T>G GRCh38
NC_000004.11:g.69512882T>G , CM000666.1:g.69512882T>G GRCh37
NC_000004.10:g.69195477T>G NCBI36
NG_052676.1:g.28613A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.1533A>C MANE Select ENSP00000341045.5:p.Lys511Asn
ENST00000338206.5:c.1533A>C ENSP00000341045.5:p.Lys511Asn
ENST00000616841.4:c.1533A>C ENSP00000482004.1:p.Lys511Asn
NM_001076.3:c.1533A>C NP_001067.2:p.Lys511Asn
NM_001076.4:c.1533A>C MANE Select NP_001067.2:p.Lys511Asn