Canonical Allele Identifier: CA357082977
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs576555278
MyVariant Identifiers: chr4:g.69512862C>G (hg19) chr4:g.68647144C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647144C>G , CM000666.2:g.68647144C>G GRCh38
NC_000004.11:g.69512862C>G , CM000666.1:g.69512862C>G GRCh37
NC_000004.10:g.69195457C>G NCBI36
NG_052676.1:g.28633G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.1553G>C MANE Select ENSP00000341045.5:p.Arg518Pro
ENST00000338206.5:c.1553G>C ENSP00000341045.5:p.Arg518Pro
ENST00000616841.4:c.1553G>C ENSP00000482004.1:p.Arg518Pro
NM_001076.3:c.1553G>C NP_001067.2:p.Arg518Pro
NM_001076.4:c.1553G>C MANE Select NP_001067.2:p.Arg518Pro
Search 100 bp 5'
Search 100 bp 3'