Canonical Allele Identifier: CA2670844631
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68670760-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670760T>G , CM000666.2:g.68670760T>G GRCh38
NC_000004.11:g.69536478T>G , CM000666.1:g.69536478T>G GRCh37
NC_000004.10:g.69219073T>G NCBI36
NG_052676.1:g.5017A>C

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-142A>C NP_001067.2:n.-142A>C
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