Canonical Allele Identifier: CA2670844534
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68669830-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68669830A>G , CM000666.2:g.68669830A>G GRCh38
NC_000004.11:g.69535548A>G , CM000666.1:g.69535548A>G GRCh37
NC_000004.10:g.69218143A>G NCBI36
NG_052676.1:g.5947T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.724+65T>C MANE Select ENSP00000341045.5:n.724+65T>C
ENST00000338206.5:c.724+65T>C ENSP00000341045.5:n.724+65T>C
ENST00000616841.4:c.724+65T>C ENSP00000482004.1:n.724+65T>C
NM_001076.3:c.724+65T>C NP_001067.2:n.724+65T>C
NM_001076.4:c.724+65T>C MANE Select NP_001067.2:n.724+65T>C
Search 100 bp 5'
Search 100 bp 3'