Canonical Allele Identifier: CA751769394

Gene: BCR

Linked Data

• dbSNP Id: rs1158573682
• gnomAD v3: 22-23308642-CACCCA-C
• gnomAD v4: 22-23308642-CACCCA-C
• MyVariant Identifiers: chr22:g.23650830_23650834del (hg19) ; chr22:g.23308643_23308647del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23308643_23308647del , CM000684.2:g.23308643_23308647del	GRCh38
NC_000022.10:g.23650830_23650834del , CM000684.1:g.23650830_23650834del	GRCh37
NC_000022.9:g.21980830_21980834del	NCBI36
NG_009244.1:g.133279_133283del
NG_009244.2:g.133279_133283del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.3013-781_3013-777del MANE Select	ENSP00000303507.8:n.3013-781_3013-777del
ENST00000305877.12:c.3013-781_3013-777del	ENSP00000303507.8:n.3013-781_3013-777del
ENST00000359540.7:c.2881-781_2881-777del	ENSP00000352535.3:n.2881-781_2881-777del
ENST00000398512.9:c.1709-781_1709-777del	ENSP00000381524.6:n.1709-781_1709-777del
ENST00000419722.6:n.238-781_238-777del
ENST00000475025.5:n.87-781_87-777del
ENST00000478978.5:n.294-781_294-777del
NM_004327.3:c.3013-781_3013-777del	NP_004318.3:n.3013-781_3013-777del
NM_021574.2:c.2881-781_2881-777del	NP_067585.2:n.2881-781_2881-777del
NM_004327.4:c.3013-781_3013-777del MANE Select	NP_004318.3:n.3013-781_3013-777del
NM_021574.3:c.2881-781_2881-777del	NP_067585.2:n.2881-781_2881-777del