Canonical Allele Identifier: CA2942364
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs758884951
ExAC: 4:69512888 G / C
gnomAD v2: 4-69512888-G-C
gnomAD v4: 4-68647170-G-C
MyVariant Identifiers: chr4:g.69512888G>C (hg19) chr4:g.68647170G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647170G>C , CM000666.2:g.68647170G>C GRCh38
NC_000004.11:g.69512888G>C , CM000666.1:g.69512888G>C GRCh37
NC_000004.10:g.69195483G>C NCBI36
NG_052676.1:g.28607C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.1527C>G MANE Select ENSP00000341045.5:p.Ile509Met
ENST00000338206.5:c.1527C>G ENSP00000341045.5:p.Ile509Met
ENST00000616841.4:c.1527C>G ENSP00000482004.1:p.Ile509Met
NM_001076.3:c.1527C>G NP_001067.2:p.Ile509Met
NM_001076.4:c.1527C>G MANE Select NP_001067.2:p.Ile509Met
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