Canonical Allele Identifier: CA2738029447

Gene: BCR

Linked Data

• dbSNP Id: rs2146225540

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23216315A>T , CM000684.2:g.23216315A>T	GRCh38
NC_000022.10:g.23558502A>T , CM000684.1:g.23558502A>T	GRCh37
NC_000022.9:g.21888502A>T	NCBI36
NG_009244.1:g.40951A>T
NG_009244.2:g.40951A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.1279+34076A>T MANE Select	ENSP00000303507.8:n.1279+34076A>T
ENST00000305877.12:c.1279+34076A>T	ENSP00000303507.8:n.1279+34076A>T
ENST00000359540.7:c.1279+34076A>T	ENSP00000352535.3:n.1279+34076A>T
ENST00000398512.9:c.1269+34086A>T	ENSP00000381524.6:n.1269+34086A>T
ENST00000463770.5:n.133+17930A>T
ENST00000479188.5:n.130-26503A>T
ENST00000487679.1:n.196+16963A>T
NM_004327.3:c.1279+34076A>T	NP_004318.3:n.1279+34076A>T
NM_021574.2:c.1279+34076A>T	NP_067585.2:n.1279+34076A>T
NM_004327.4:c.1279+34076A>T MANE Select	NP_004318.3:n.1279+34076A>T
NM_021574.3:c.1279+34076A>T	NP_067585.2:n.1279+34076A>T