Canonical Allele Identifier: CA2397674403

Gene: BCR

Linked Data

• dbSNP Id: rs2072582131

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23203806A>G , CM000684.2:g.23203806A>G	GRCh38
NC_000022.10:g.23545993A>G , CM000684.1:g.23545993A>G	GRCh37
NC_000022.9:g.21875993A>G	NCBI36
NG_009244.1:g.28442A>G
NG_009244.2:g.28442A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.1279+21567A>G MANE Select	ENSP00000303507.8:n.1279+21567A>G
ENST00000305877.12:c.1279+21567A>G	ENSP00000303507.8:n.1279+21567A>G
ENST00000359540.7:c.1279+21567A>G	ENSP00000352535.3:n.1279+21567A>G
ENST00000398512.9:c.1269+21577A>G	ENSP00000381524.6:n.1269+21577A>G
ENST00000463770.5:n.133+5421A>G
ENST00000479188.5:n.129+23974A>G
ENST00000487679.1:n.196+4454A>G
NM_004327.3:c.1279+21567A>G	NP_004318.3:n.1279+21567A>G
NM_021574.2:c.1279+21567A>G	NP_067585.2:n.1279+21567A>G
NM_004327.4:c.1279+21567A>G MANE Select	NP_004318.3:n.1279+21567A>G
NM_021574.3:c.1279+21567A>G	NP_067585.2:n.1279+21567A>G