Canonical Allele Identifier: CA914677899

Gene: BCR

Linked Data

• dbSNP Id: rs1568985521
• gnomAD v2: 22-23650953-C-A
• gnomAD v3: 22-23308766-C-A
• gnomAD v4: 22-23308766-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23308766C>A , CM000684.2:g.23308766C>A	GRCh38
NC_000022.10:g.23650953C>A , CM000684.1:g.23650953C>A	GRCh37
NC_000022.9:g.21980953C>A	NCBI36
NG_009244.1:g.133402C>A
NG_009244.2:g.133402C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.3013-658C>A MANE Select	ENSP00000303507.8:n.3013-658C>A
ENST00000305877.12:c.3013-658C>A	ENSP00000303507.8:n.3013-658C>A
ENST00000359540.7:c.2881-658C>A	ENSP00000352535.3:n.2881-658C>A
ENST00000398512.9:c.1709-658C>A	ENSP00000381524.6:n.1709-658C>A
ENST00000419722.6:n.238-658C>A
ENST00000475025.5:n.87-658C>A
ENST00000478978.5:n.294-658C>A
NM_004327.3:c.3013-658C>A	NP_004318.3:n.3013-658C>A
NM_021574.2:c.2881-658C>A	NP_067585.2:n.2881-658C>A
NM_004327.4:c.3013-658C>A MANE Select	NP_004318.3:n.3013-658C>A
NM_021574.3:c.2881-658C>A	NP_067585.2:n.2881-658C>A