Canonical Allele Identifier: CA1465820694
Gene: UGT2B15 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646628C= , CM000666.2:g.68646628C= GRCh38
NC_000004.11:g.69512346C= , CM000666.1:g.69512346C= GRCh37
NC_000004.10:g.69194941C= NCBI36
NG_052676.1:g.29149G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*476G= MANE Select ENSP00000341045.5:n.*476G=
ENST00000616841.4:c.1732+337G= ENSP00000482004.1:n.1732+337G=
NM_001076.3:c.*476G= NP_001067.2:n.*476G=
NM_001076.4:c.*476G= MANE Select NP_001067.2:n.*476G=
Search 100 bp 5'
Search 100 bp 3'