Canonical Allele Identifier: CA98760105
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs890906202
MyVariant Identifiers: chr4:g.69535824G>T (hg19) chr4:g.68670106G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670106G>T , CM000666.2:g.68670106G>T GRCh38
NC_000004.11:g.69535824G>T , CM000666.1:g.69535824G>T GRCh37
NC_000004.10:g.69218419G>T NCBI36
NG_052676.1:g.5671C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.513C>A MANE Select ENSP00000341045.5:p.Tyr171Ter
ENST00000338206.5:c.513C>A ENSP00000341045.5:p.Tyr171Ter
ENST00000616841.4:c.513C>A ENSP00000482004.1:p.Tyr171Ter
NM_001076.3:c.513C>A NP_001067.2:p.Tyr171Ter
NM_001076.4:c.513C>A MANE Select NP_001067.2:p.Tyr171Ter
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