Canonical Allele Identifier: CA797795760
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1480858904
MyVariant Identifiers: chr4:g.69536357C>G (hg19) chr4:g.68670639C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670639C>G , CM000666.2:g.68670639C>G GRCh38
NC_000004.11:g.69536357C>G , CM000666.1:g.69536357C>G GRCh37
NC_000004.10:g.69218952C>G NCBI36
NG_052676.1:g.5138G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.-21G>C MANE Select ENSP00000341045.5:n.-21G>C
NM_001076.3:c.-21G>C NP_001067.2:n.-21G>C
NM_001076.4:c.-21G>C MANE Select NP_001067.2:n.-21G>C
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