Canonical Allele Identifier: CA98747958
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs75243135
MyVariant Identifiers: chr4:g.69512905T>C (hg19) chr4:g.68647187T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647187T>C , CM000666.2:g.68647187T>C GRCh38
NC_000004.11:g.69512905T>C , CM000666.1:g.69512905T>C GRCh37
NC_000004.10:g.69195500T>C NCBI36
NG_052676.1:g.28590A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.1510A>G MANE Select ENSP00000341045.5:p.Thr504Ala
ENST00000338206.5:c.1510A>G ENSP00000341045.5:p.Thr504Ala
ENST00000616841.4:c.1510A>G ENSP00000482004.1:p.Thr504Ala
NM_001076.3:c.1510A>G NP_001067.2:p.Thr504Ala
NM_001076.4:c.1510A>G MANE Select NP_001067.2:p.Thr504Ala
Search 100 bp 5'
Search 100 bp 3'