Canonical Allele Identifier: CA357086805
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68670386-G-A
MyVariant Identifiers: chr4:g.69536104G>A (hg19) chr4:g.68670386G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670386G>A , CM000666.2:g.68670386G>A GRCh38
NC_000004.11:g.69536104G>A , CM000666.1:g.69536104G>A GRCh37
NC_000004.10:g.69218699G>A NCBI36
NG_052676.1:g.5391C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.233C>T MANE Select ENSP00000341045.5:p.Pro78Leu
ENST00000338206.5:c.233C>T ENSP00000341045.5:p.Pro78Leu
ENST00000616841.4:c.233C>T ENSP00000482004.1:p.Pro78Leu
NM_001076.3:c.233C>T NP_001067.2:p.Pro78Leu
NM_001076.4:c.233C>T MANE Select NP_001067.2:p.Pro78Leu
Search 100 bp 5'
Search 100 bp 3'