Canonical Allele Identifier: CA797777200
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1264882023
MyVariant Identifiers: chr4:g.69512387C>T (hg19) chr4:g.68646669C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646669C>T , CM000666.2:g.68646669C>T GRCh38
NC_000004.11:g.69512387C>T , CM000666.1:g.69512387C>T GRCh37
NC_000004.10:g.69194982C>T NCBI36
NG_052676.1:g.29108G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*435G>A MANE Select ENSP00000341045.5:n.*435G>A
ENST00000338206.5:c.*435G>A ENSP00000341045.5:n.*435G>A
ENST00000616841.4:c.1732+296G>A ENSP00000482004.1:n.1732+296G>A
NM_001076.3:c.*435G>A NP_001067.2:n.*435G>A
NM_001076.4:c.*435G>A MANE Select NP_001067.2:n.*435G>A
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