Canonical Allele Identifier: CA98747630
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1006415181
gnomAD v2: 4-69512546-G-A
gnomAD v3: 4-68646828-G-A
gnomAD v4: 4-68646828-G-A
MyVariant Identifiers: chr4:g.69512546G>A (hg19) chr4:g.68646828G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646828G>A , CM000666.2:g.68646828G>A GRCh38
NC_000004.11:g.69512546G>A , CM000666.1:g.69512546G>A GRCh37
NC_000004.10:g.69195141G>A NCBI36
NG_052676.1:g.28949C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*276C>T MANE Select ENSP00000341045.5:n.*276C>T
ENST00000338206.5:c.*276C>T ENSP00000341045.5:n.*276C>T
ENST00000616841.4:c.1732+137C>T ENSP00000482004.1:n.1732+137C>T
NM_001076.3:c.*276C>T NP_001067.2:n.*276C>T
NM_001076.4:c.*276C>T MANE Select NP_001067.2:n.*276C>T
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