Canonical Allele Identifier: CA439705814
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68670595-G-A
MyVariant Identifiers: chr4:g.69536313G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670595G>A , CM000666.2:g.68670595G>A GRCh38
NC_000004.11:g.69536313G>A , CM000666.1:g.69536313G>A GRCh37
NC_000004.10:g.69218908G>A NCBI36
NG_052676.1:g.5182C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.24C>T MANE Select ENSP00000341045.5:p.Val8=
ENST00000338206.5:c.24C>T ENSP00000341045.5:p.Val8=
ENST00000616841.4:c.24C>T ENSP00000482004.1:p.Val8=
NM_001076.3:c.24C>T NP_001067.2:p.Val8=
NM_001076.4:c.24C>T MANE Select NP_001067.2:p.Val8=
Search 100 bp 5'
Search 100 bp 3'