Canonical Allele Identifier: CA357085131
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1329524939
gnomAD v2: 4-69535738-G-C
gnomAD v4: 4-68670020-G-C
MyVariant Identifiers: chr4:g.69535738G>C (hg19) chr4:g.68670020G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670020G>C , CM000666.2:g.68670020G>C GRCh38
NC_000004.11:g.69535738G>C , CM000666.1:g.69535738G>C GRCh37
NC_000004.10:g.69218333G>C NCBI36
NG_052676.1:g.5757C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.599C>G MANE Select ENSP00000341045.5:p.Ser200Ter
ENST00000338206.5:c.599C>G ENSP00000341045.5:p.Ser200Ter
ENST00000616841.4:c.599C>G ENSP00000482004.1:p.Ser200Ter
NM_001076.3:c.599C>G NP_001067.2:p.Ser200Ter
NM_001076.4:c.599C>G MANE Select NP_001067.2:p.Ser200Ter
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