Canonical Allele Identifier: CA1465820937
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1732493705
gnomAD v4: 4-68647013-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647013G>C , CM000666.2:g.68647013G>C GRCh38
NC_000004.11:g.69512731G>C , CM000666.1:g.69512731G>C GRCh37
NC_000004.10:g.69195326G>C NCBI36
NG_052676.1:g.28764C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*91C>G MANE Select ENSP00000341045.5:n.*91C>G
ENST00000338206.5:c.*91C>G ENSP00000341045.5:n.*91C>G
ENST00000616841.4:c.1684C>G ENSP00000482004.1:n.1684C>G
NM_001076.3:c.*91C>G NP_001067.2:n.*91C>G
NM_001076.4:c.*91C>G MANE Select NP_001067.2:n.*91C>G
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