Canonical Allele Identifier: CA552612250
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1560612881
gnomAD v2: 4-69535603-C-G
gnomAD v4: 4-68669885-C-G
MyVariant Identifiers: chr4:g.69535603_69535605delinsGAT (hg19) chr4:g.68669885_68669887delinsGAT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68669885C>G , CM000666.2:g.68669885C>G GRCh38
NC_000004.11:g.69535603C>G , CM000666.1:g.69535603C>G GRCh37
NC_000004.10:g.69218198C>G NCBI36
NG_052676.1:g.5892G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.724+10G>C MANE Select ENSP00000341045.5:n.724+10G>C
ENST00000338206.5:c.724+10G>C ENSP00000341045.5:n.724+10G>C
ENST00000616841.4:c.724+10G>C ENSP00000482004.1:n.724+10G>C
NM_001076.3:c.724+10G>C NP_001067.2:n.724+10G>C
NM_001076.4:c.724+10G>C MANE Select NP_001067.2:n.724+10G>C
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