Canonical Allele Identifier: CA2670843468
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68646798-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646798G>A , CM000666.2:g.68646798G>A GRCh38
NC_000004.11:g.69512516G>A , CM000666.1:g.69512516G>A GRCh37
NC_000004.10:g.69195111G>A NCBI36
NG_052676.1:g.28979C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*306C>T MANE Select ENSP00000341045.5:n.*306C>T
ENST00000338206.5:c.*306C>T ENSP00000341045.5:n.*306C>T
ENST00000616841.4:c.1732+167C>T ENSP00000482004.1:n.1732+167C>T
NM_001076.3:c.*306C>T NP_001067.2:n.*306C>T
NM_001076.4:c.*306C>T MANE Select NP_001067.2:n.*306C>T
Search 100 bp 5'
Search 100 bp 3'