Canonical Allele Identifier: CA357083050
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68647178-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647178A>G , CM000666.2:g.68647178A>G GRCh38
NC_000004.11:g.69512896A>G , CM000666.1:g.69512896A>G GRCh37
NC_000004.10:g.69195491A>G NCBI36
NG_052676.1:g.28599T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.1519T>C MANE Select ENSP00000341045.5:p.Phe507Leu
ENST00000338206.5:c.1519T>C ENSP00000341045.5:p.Phe507Leu
ENST00000616841.4:c.1519T>C ENSP00000482004.1:p.Phe507Leu
NM_001076.3:c.1519T>C NP_001067.2:p.Phe507Leu
NM_001076.4:c.1519T>C MANE Select NP_001067.2:p.Phe507Leu