Canonical Allele Identifier: CA552612219
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs371051201
gnomAD v2: 4-69512819-T-G
gnomAD v4: 4-68647101-T-G
MyVariant Identifiers: chr4:g.69512819T>G (hg19) chr4:g.68647101T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647101T>G , CM000666.2:g.68647101T>G GRCh38
NC_000004.11:g.69512819T>G , CM000666.1:g.69512819T>G GRCh37
NC_000004.10:g.69195414T>G NCBI36
NG_052676.1:g.28676A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*3A>C MANE Select ENSP00000341045.5:n.*3A>C
ENST00000338206.5:c.*3A>C ENSP00000341045.5:n.*3A>C
ENST00000616841.4:c.1596A>C ENSP00000482004.1:n.1596A>C
NM_001076.3:c.*3A>C NP_001067.2:n.*3A>C
NM_001076.4:c.*3A>C MANE Select NP_001067.2:n.*3A>C
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