Canonical Allele Identifier: CA2670847366

Gene: UGT2B10

Linked Data

• gnomAD v4: 4-68816789-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68816789G>T , CM000666.2:g.68816789G>T	GRCh38
NC_000004.11:g.69682507G>T , CM000666.1:g.69682507G>T	GRCh37
NC_000004.10:g.69717096G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265403.12:c.718+52G>T MANE Select	ENSP00000265403.7:n.718+52G>T
ENST00000265403.11:c.718+52G>T	ENSP00000265403.7:n.718+52G>T
ENST00000458688.2:c.466+304G>T	ENSP00000413420.2:n.466+304G>T
NM_001075.5:c.718+52G>T	NP_001066.1:n.718+52G>T
NM_001144767.2:c.466+304G>T	NP_001138239.1:n.466+304G>T
NM_001290091.1:c.-27+617G>T	NP_001277020.1:n.-27+617G>T
XM_017008585.2:c.718+52G>T	XP_016864074.1:n.718+52G>T
NM_001075.6:c.718+52G>T MANE Select	NP_001066.1:n.718+52G>T
NM_001144767.3:c.466+304G>T	NP_001138239.1:n.466+304G>T
NM_001290091.2:c.-27+617G>T	NP_001277020.1:n.-27+617G>T