Canonical Allele Identifier: CA98747411
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1019476895
MyVariant Identifiers: chr4:g.69512311C>T (hg19) chr4:g.68646593C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646593C>T , CM000666.2:g.68646593C>T GRCh38
NC_000004.11:g.69512311C>T , CM000666.1:g.69512311C>T GRCh37
NC_000004.10:g.69194906C>T NCBI36
NG_052676.1:g.29184G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000616841.4:c.1732+372G>A ENSP00000482004.1:n.1732+372G>A
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