Canonical Allele Identifier: CA2670843383
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68646698-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646698T>G , CM000666.2:g.68646698T>G GRCh38
NC_000004.11:g.69512416T>G , CM000666.1:g.69512416T>G GRCh37
NC_000004.10:g.69195011T>G NCBI36
NG_052676.1:g.29079A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*406A>C MANE Select ENSP00000341045.5:n.*406A>C
ENST00000338206.5:c.*406A>C ENSP00000341045.5:n.*406A>C
ENST00000616841.4:c.1732+267A>C ENSP00000482004.1:n.1732+267A>C
NM_001076.3:c.*406A>C NP_001067.2:n.*406A>C
NM_001076.4:c.*406A>C MANE Select NP_001067.2:n.*406A>C
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