Canonical Allele Identifier: CA439935389
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1733271042
gnomAD v4: 4-68670307-A-G
MyVariant Identifiers: chr4:g.69536025A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670307A>G , CM000666.2:g.68670307A>G GRCh38
NC_000004.11:g.69536025A>G , CM000666.1:g.69536025A>G GRCh37
NC_000004.10:g.69218620A>G NCBI36
NG_052676.1:g.5470T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.312T>C MANE Select ENSP00000341045.5:p.Asn104=
ENST00000338206.5:c.312T>C ENSP00000341045.5:p.Asn104=
ENST00000616841.4:c.312T>C ENSP00000482004.1:p.Asn104=
NM_001076.3:c.312T>C NP_001067.2:p.Asn104=
NM_001076.4:c.312T>C MANE Select NP_001067.2:p.Asn104=