Canonical Allele Identifier: CA552612258
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1235923953
gnomAD v2: 4-69535962-G-GAAT
gnomAD v4: 4-68670244-G-GAAT
MyVariant Identifiers: chr4:g.69535962_69535963insAAT (hg19) chr4:g.68670244_68670245insAAT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670244_68670245insAAT , CM000666.2:g.68670244_68670245insAAT GRCh38
NC_000004.11:g.69535962_69535963insAAT , CM000666.1:g.69535962_69535963insAAT GRCh37
NC_000004.10:g.69218557_69218558insAAT NCBI36
NG_052676.1:g.5532_5533insATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.374_375insATT MANE Select ENSP00000341045.5:p.Asn125delinsLysPhe
ENST00000338206.5:c.374_375insATT ENSP00000341045.5:p.Asn125delinsLysPhe
ENST00000616841.4:c.374_375insATT ENSP00000482004.1:p.Asn125delinsLysPhe
NM_001076.3:c.374_375insATT NP_001067.2:p.Asn125delinsLysPhe
NM_001076.4:c.374_375insATT MANE Select NP_001067.2:p.Asn125delinsLysPhe
Search 100 bp 5'
Search 100 bp 3'