Canonical Allele Identifier: CA357082922
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68647119-C-G
MyVariant Identifiers: chr4:g.69512837C>G (hg19) chr4:g.68647119C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647119C>G , CM000666.2:g.68647119C>G GRCh38
NC_000004.11:g.69512837C>G , CM000666.1:g.69512837C>G GRCh37
NC_000004.10:g.69195432C>G NCBI36
NG_052676.1:g.28658G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.1578G>C MANE Select ENSP00000341045.5:p.Lys526Asn
ENST00000338206.5:c.1578G>C ENSP00000341045.5:p.Lys526Asn
ENST00000616841.4:c.1578G>C ENSP00000482004.1:p.Lys526Asn
NM_001076.3:c.1578G>C NP_001067.2:p.Lys526Asn
NM_001076.4:c.1578G>C MANE Select NP_001067.2:p.Lys526Asn
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