Canonical Allele Identifier: CA2670843359
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68646601-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646601G>C , CM000666.2:g.68646601G>C GRCh38
NC_000004.11:g.69512319G>C , CM000666.1:g.69512319G>C GRCh37
NC_000004.10:g.69194914G>C NCBI36
NG_052676.1:g.29176C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*503C>G MANE Select ENSP00000341045.5:n.*503C>G
ENST00000616841.4:c.1732+364C>G ENSP00000482004.1:n.1732+364C>G
NM_001076.3:c.*503C>G NP_001067.2:n.*503C>G
NM_001076.4:c.*503C>G MANE Select NP_001067.2:n.*503C>G
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