Canonical Allele Identifier: CA2670843522
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68646863-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646863T>C , CM000666.2:g.68646863T>C GRCh38
NC_000004.11:g.69512581T>C , CM000666.1:g.69512581T>C GRCh37
NC_000004.10:g.69195176T>C NCBI36
NG_052676.1:g.28914A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*241A>G MANE Select ENSP00000341045.5:n.*241A>G
ENST00000338206.5:c.*241A>G ENSP00000341045.5:n.*241A>G
ENST00000616841.4:c.1732+102A>G ENSP00000482004.1:n.1732+102A>G
NM_001076.3:c.*241A>G NP_001067.2:n.*241A>G
NM_001076.4:c.*241A>G MANE Select NP_001067.2:n.*241A>G
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