Canonical Allele Identifier: CA2943009

Gene: UGT2B10

Linked Data

• dbSNP Id: rs772784724
• ExAC: 4:69682479 C / T
• gnomAD v2: 4-69682479-C-T
• gnomAD v3: 4-68816761-C-T
• gnomAD v4: 4-68816761-C-T
• MyVariant Identifiers: chr4:g.69682479C>T (hg19) ; chr4:g.68816761C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68816761C>T , CM000666.2:g.68816761C>T	GRCh38
NC_000004.11:g.69682479C>T , CM000666.1:g.69682479C>T	GRCh37
NC_000004.10:g.69717068C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265403.12:c.718+24C>T MANE Select	ENSP00000265403.7:n.718+24C>T
ENST00000265403.11:c.718+24C>T	ENSP00000265403.7:n.718+24C>T
ENST00000458688.2:c.466+276C>T	ENSP00000413420.2:n.466+276C>T
NM_001075.5:c.718+24C>T	NP_001066.1:n.718+24C>T
NM_001144767.2:c.466+276C>T	NP_001138239.1:n.466+276C>T
NM_001290091.1:c.-27+589C>T	NP_001277020.1:n.-27+589C>T
XM_017008585.2:c.718+24C>T	XP_016864074.1:n.718+24C>T
NM_001075.6:c.718+24C>T MANE Select	NP_001066.1:n.718+24C>T
NM_001144767.3:c.466+276C>T	NP_001138239.1:n.466+276C>T
NM_001290091.2:c.-27+589C>T	NP_001277020.1:n.-27+589C>T