Canonical Allele Identifier: CA2397697586

Gene: BCR

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23250864G>C , CM000684.2:g.23250864G>C	GRCh38
NC_000022.10:g.23593051G>C , CM000684.1:g.23593051G>C	GRCh37
NC_000022.9:g.21923051G>C	NCBI36
NG_009244.1:g.75500G>C
NG_009244.2:g.75500G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.1280-2935G>C MANE Select	ENSP00000303507.8:n.1280-2935G>C
ENST00000305877.12:c.1280-2935G>C	ENSP00000303507.8:n.1280-2935G>C
ENST00000359540.7:c.1280-2935G>C	ENSP00000352535.3:n.1280-2935G>C
ENST00000398512.9:c.1270-37280G>C	ENSP00000381524.6:n.1270-37280G>C
ENST00000463770.5:n.134-2935G>C
ENST00000479188.5:n.298-2935G>C
ENST00000487679.1:n.197-2935G>C
NM_004327.3:c.1280-2935G>C	NP_004318.3:n.1280-2935G>C
NM_021574.2:c.1280-2935G>C	NP_067585.2:n.1280-2935G>C
NM_004327.4:c.1280-2935G>C MANE Select	NP_004318.3:n.1280-2935G>C
NM_021574.3:c.1280-2935G>C	NP_067585.2:n.1280-2935G>C