Canonical Allele Identifier: CA751769385

Gene: BCR

Linked Data

• dbSNP Id: rs1299152659
• gnomAD v3: 22-23308630-GTACTGC-G
• gnomAD v4: 22-23308630-GTACTGC-G
• MyVariant Identifiers: chr22:g.23650818_23650823del (hg19) ; chr22:g.23308631_23308636del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23308632_23308637del , CM000684.2:g.23308632_23308637del	GRCh38
NC_000022.10:g.23650819_23650824del , CM000684.1:g.23650819_23650824del	GRCh37
NC_000022.9:g.21980819_21980824del	NCBI36
NG_009244.1:g.133268_133273del
NG_009244.2:g.133268_133273del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.3013-792_3013-787del MANE Select	ENSP00000303507.8:n.3013-792_3013-787del
ENST00000305877.12:c.3013-792_3013-787del	ENSP00000303507.8:n.3013-792_3013-787del
ENST00000359540.7:c.2881-792_2881-787del	ENSP00000352535.3:n.2881-792_2881-787del
ENST00000398512.9:c.1709-792_1709-787del	ENSP00000381524.6:n.1709-792_1709-787del
ENST00000419722.6:n.238-792_238-787del
ENST00000475025.5:n.87-792_87-787del
ENST00000478978.5:n.294-792_294-787del
NM_004327.3:c.3013-792_3013-787del	NP_004318.3:n.3013-792_3013-787del
NM_021574.2:c.2881-792_2881-787del	NP_067585.2:n.2881-792_2881-787del
NM_004327.4:c.3013-792_3013-787del MANE Select	NP_004318.3:n.3013-792_3013-787del
NM_021574.3:c.2881-792_2881-787del	NP_067585.2:n.2881-792_2881-787del