Canonical Allele Identifier: CA2397726731

Gene: BCR

Linked Data

• dbSNP Id: rs2073972849

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23308538_23308547del , CM000684.2:g.23308538_23308547del	GRCh38
NC_000022.10:g.23650725_23650734del , CM000684.1:g.23650725_23650734del	GRCh37
NC_000022.9:g.21980725_21980734del	NCBI36
NG_009244.1:g.133174_133183del
NG_009244.2:g.133174_133183del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.3013-886_3013-877del MANE Select	ENSP00000303507.8:n.3013-886_3013-877del
ENST00000305877.12:c.3013-886_3013-877del	ENSP00000303507.8:n.3013-886_3013-877del
ENST00000359540.7:c.2881-886_2881-877del	ENSP00000352535.3:n.2881-886_2881-877del
ENST00000398512.9:c.1709-886_1709-877del	ENSP00000381524.6:n.1709-886_1709-877del
ENST00000419722.6:n.238-886_238-877del
ENST00000475025.5:n.87-886_87-877del
ENST00000478978.5:n.293+774_293+783del
NM_004327.3:c.3013-886_3013-877del	NP_004318.3:n.3013-886_3013-877del
NM_021574.2:c.2881-886_2881-877del	NP_067585.2:n.2881-886_2881-877del
NM_004327.4:c.3013-886_3013-877del MANE Select	NP_004318.3:n.3013-886_3013-877del
NM_021574.3:c.2881-886_2881-877del	NP_067585.2:n.2881-886_2881-877del