Canonical Allele Identifier: CA2670843432
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1732484365
gnomAD v4: 4-68646769-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646769T>C , CM000666.2:g.68646769T>C GRCh38
NC_000004.11:g.69512487T>C , CM000666.1:g.69512487T>C GRCh37
NC_000004.10:g.69195082T>C NCBI36
NG_052676.1:g.29008A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*335A>G MANE Select ENSP00000341045.5:n.*335A>G
ENST00000338206.5:c.*335A>G ENSP00000341045.5:n.*335A>G
ENST00000616841.4:c.1732+196A>G ENSP00000482004.1:n.1732+196A>G
NM_001076.3:c.*335A>G NP_001067.2:n.*335A>G
NM_001076.4:c.*335A>G MANE Select NP_001067.2:n.*335A>G
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Search 100 bp 3'