Canonical Allele Identifier: CA1024450061

Gene: BCR

Linked Data

• dbSNP Id: rs2072581898

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23203782T>G , CM000684.2:g.23203782T>G	GRCh38
NC_000022.10:g.23545969T>G , CM000684.1:g.23545969T>G	GRCh37
NC_000022.9:g.21875969T>G	NCBI36
NG_009244.1:g.28418T>G
NG_009244.2:g.28418T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000305877.13:c.1279+21543T>G MANE Select	ENSP00000303507.8:n.1279+21543T>G
ENST00000305877.12:c.1279+21543T>G	ENSP00000303507.8:n.1279+21543T>G
ENST00000359540.7:c.1279+21543T>G	ENSP00000352535.3:n.1279+21543T>G
ENST00000398512.9:c.1269+21553T>G	ENSP00000381524.6:n.1269+21553T>G
ENST00000463770.5:n.133+5397T>G
ENST00000479188.5:n.129+23950T>G
ENST00000487679.1:n.196+4430T>G
NM_004327.3:c.1279+21543T>G	NP_004318.3:n.1279+21543T>G
NM_021574.2:c.1279+21543T>G	NP_067585.2:n.1279+21543T>G
NM_004327.4:c.1279+21543T>G MANE Select	NP_004318.3:n.1279+21543T>G
NM_021574.3:c.1279+21543T>G	NP_067585.2:n.1279+21543T>G