Canonical Allele Identifier: CA357083085
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68647196-A-G
MyVariant Identifiers: chr4:g.69512914A>G (hg19) chr4:g.68647196A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647196A>G , CM000666.2:g.68647196A>G GRCh38
NC_000004.11:g.69512914A>G , CM000666.1:g.69512914A>G GRCh37
NC_000004.10:g.69195509A>G NCBI36
NG_052676.1:g.28581T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.1501T>C MANE Select ENSP00000341045.5:p.Cys501Arg
ENST00000338206.5:c.1501T>C ENSP00000341045.5:p.Cys501Arg
ENST00000616841.4:c.1501T>C ENSP00000482004.1:p.Cys501Arg
NM_001076.3:c.1501T>C NP_001067.2:p.Cys501Arg
NM_001076.4:c.1501T>C MANE Select NP_001067.2:p.Cys501Arg
Search 100 bp 5'
Search 100 bp 3'