Canonical Allele Identifier: CA2589573568

Gene: BCR

Linked Data

• dbSNP Id: rs2146323035
• gnomAD v3: 22-23305671-GCCAGGCC-G
• gnomAD v4: 22-23305671-GCCAGGCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23305673_23305679del , CM000684.2:g.23305673_23305679del	GRCh38
NC_000022.10:g.23647860_23647866del , CM000684.1:g.23647860_23647866del	GRCh37
NC_000022.9:g.21977860_21977866del	NCBI36
NG_009244.1:g.130309_130315del
NG_009244.2:g.130309_130315del

Transcript Alleles

HGVS	Amino-acid change
ENST00000305877.13:c.3013-3751_3013-3745del MANE Select	ENSP00000303507.8:n.3013-3751_3013-3745del
ENST00000305877.12:c.3013-3751_3013-3745del	ENSP00000303507.8:n.3013-3751_3013-3745del
ENST00000359540.7:c.2881-3751_2881-3745del	ENSP00000352535.3:n.2881-3751_2881-3745del
ENST00000398512.9:c.1709-3751_1709-3745del	ENSP00000381524.6:n.1709-3751_1709-3745del
ENST00000419722.6:n.238-3751_238-3745del
NM_004327.3:c.3013-3751_3013-3745del	NP_004318.3:n.3013-3751_3013-3745del
NM_021574.2:c.2881-3751_2881-3745del	NP_067585.2:n.2881-3751_2881-3745del
NM_004327.4:c.3013-3751_3013-3745del MANE Select	NP_004318.3:n.3013-3751_3013-3745del
NM_021574.3:c.2881-3751_2881-3745del	NP_067585.2:n.2881-3751_2881-3745del