Canonical Allele Identifier: CA340951926

Gene: BCL10

Linked Data

• dbSNP Id: rs1660352619
• gnomAD v4: 1-85270839-C-T
• MyVariant Identifiers: chr1:g.85736522C>T (hg19) ; chr1:g.85270839C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.85270839C>T , CM000663.2:g.85270839C>T	GRCh38
NC_000001.10:g.85736522C>T , CM000663.1:g.85736522C>T	GRCh37
NC_000001.9:g.85509110C>T	NCBI36
NG_012216.1:g.12062G>A
NG_012216.2:g.11066G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620248.3:c.125G>A	ENSP00000480561.2:p.Arg42His
ENST00000620248.2:c.125G>A	ENSP00000480561.2:p.Arg42His
ENST00000648566.1:c.125G>A MANE Select	ENSP00000498104.1:p.Arg42His
ENST00000649060.1:c.*1234G>A	ENSP00000497490.1:n.*1234G>A
ENST00000649434.1:n.191G>A
ENST00000650582.1:n.656G>A
ENST00000370580.5:c.125G>A	ENSP00000359612.1:p.Arg42His
ENST00000620248.1:c.125G>A	ENSP00000480561.1:p.Arg42His
NM_003921.4:c.125G>A	NP_003912.1:p.Arg42His
XM_005271311.2:c.125G>A	XP_005271368.1:p.Arg42His
XM_011542397.1:c.284G>A	XP_011540699.1:p.Arg95His
XM_011542398.1:c.284G>A	XP_011540700.1:p.Arg95His
XM_011542399.1:c.71G>A	XP_011540701.1:p.Arg24His
NM_001320715.1:c.125G>A	NP_001307644.1:p.Arg42His
NM_003921.5:c.125G>A MANE Select	NP_003912.1:p.Arg42His
XM_011542397.3:c.284G>A	XP_011540699.1:p.Arg95His
XM_011542398.2:c.284G>A	XP_011540700.1:p.Arg95His
XM_011542399.2:c.71G>A	XP_011540701.1:p.Arg24His
NM_001320715.2:c.125G>A	NP_001307644.1:p.Arg42His