Canonical Allele Identifier: CA357082962
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68647136-C-T
MyVariant Identifiers: chr4:g.69512854C>T (hg19) chr4:g.68647136C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647136C>T , CM000666.2:g.68647136C>T GRCh38
NC_000004.11:g.69512854C>T , CM000666.1:g.69512854C>T GRCh37
NC_000004.10:g.69195449C>T NCBI36
NG_052676.1:g.28641G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.1561G>A MANE Select ENSP00000341045.5:p.Ala521Thr
ENST00000338206.5:c.1561G>A ENSP00000341045.5:p.Ala521Thr
ENST00000616841.4:c.1561G>A ENSP00000482004.1:p.Ala521Thr
NM_001076.3:c.1561G>A NP_001067.2:p.Ala521Thr
NM_001076.4:c.1561G>A MANE Select NP_001067.2:p.Ala521Thr
Search 100 bp 5'
Search 100 bp 3'