Canonical Allele Identifier: CA2670844580
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68670640-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670640T>G , CM000666.2:g.68670640T>G GRCh38
NC_000004.11:g.69536358T>G , CM000666.1:g.69536358T>G GRCh37
NC_000004.10:g.69218953T>G NCBI36
NG_052676.1:g.5137A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.-22A>C MANE Select ENSP00000341045.5:n.-22A>C
NM_001076.3:c.-22A>C NP_001067.2:n.-22A>C
NM_001076.4:c.-22A>C MANE Select NP_001067.2:n.-22A>C
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