Canonical Allele Identifier: CA797777170
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1553923816
gnomAD v3: 4-68646638-T-TA
gnomAD v4: 4-68646638-T-TA
MyVariant Identifiers: chr4:g.69512356_69512357insA (hg19) chr4:g.68646638_68646639insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646639dup , CM000666.2:g.68646639dup GRCh38
NC_000004.11:g.69512357dup , CM000666.1:g.69512357dup GRCh37
NC_000004.10:g.69194952dup NCBI36
NG_052676.1:g.29138dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*465dup MANE Select ENSP00000341045.5:n.*465dup
ENST00000338206.5:c.*465dup ENSP00000341045.5:n.*465dup
ENST00000616841.4:c.1732+326dup ENSP00000482004.1:n.1732+326dup
NM_001076.3:c.*465dup NP_001067.2:n.*465dup
NM_001076.4:c.*465dup MANE Select NP_001067.2:n.*465dup
Search 100 bp 5'
Search 100 bp 3'