Canonical Allele Identifier: CA751769555

Gene: BCR

Linked Data

• dbSNP Id: rs1354680303
• gnomAD v3: 22-23308937-TTC-T
• gnomAD v4: 22-23308937-TTC-T
• MyVariant Identifiers: chr22:g.23651125_23651126del (hg19) ; chr22:g.23308938_23308939del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23308939_23308940del , CM000684.2:g.23308939_23308940del	GRCh38
NC_000022.10:g.23651126_23651127del , CM000684.1:g.23651126_23651127del	GRCh37
NC_000022.9:g.21981126_21981127del	NCBI36
NG_009244.1:g.133575_133576del
NG_009244.2:g.133575_133576del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.3013-485_3013-484del MANE Select	ENSP00000303507.8:n.3013-485_3013-484del
ENST00000305877.12:c.3013-485_3013-484del	ENSP00000303507.8:n.3013-485_3013-484del
ENST00000359540.7:c.2881-485_2881-484del	ENSP00000352535.3:n.2881-485_2881-484del
ENST00000398512.9:c.1709-485_1709-484del	ENSP00000381524.6:n.1709-485_1709-484del
ENST00000419722.6:n.238-485_238-484del
ENST00000475025.5:n.87-485_87-484del
ENST00000478978.5:n.294-485_294-484del
NM_004327.3:c.3013-485_3013-484del	NP_004318.3:n.3013-485_3013-484del
NM_021574.2:c.2881-485_2881-484del	NP_067585.2:n.2881-485_2881-484del
NM_004327.4:c.3013-485_3013-484del MANE Select	NP_004318.3:n.3013-485_3013-484del
NM_021574.3:c.2881-485_2881-484del	NP_067585.2:n.2881-485_2881-484del