Canonical Allele Identifier: CA1063752313
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1315688424
gnomAD v3: 4-68646628-C-T
gnomAD v4: 4-68646628-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646628C>T , CM000666.2:g.68646628C>T GRCh38
NC_000004.11:g.69512346C>T , CM000666.1:g.69512346C>T GRCh37
NC_000004.10:g.69194941C>T NCBI36
NG_052676.1:g.29149G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*476G>A MANE Select ENSP00000341045.5:n.*476G>A
ENST00000616841.4:c.1732+337G>A ENSP00000482004.1:n.1732+337G>A
NM_001076.3:c.*476G>A NP_001067.2:n.*476G>A
NM_001076.4:c.*476G>A MANE Select NP_001067.2:n.*476G>A
Search 100 bp 5'
Search 100 bp 3'