Canonical Allele Identifier: CA2738030695

Gene: BCR

Linked Data

• dbSNP Id: rs2146322996

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23305630G>A , CM000684.2:g.23305630G>A	GRCh38
NC_000022.10:g.23647817G>A , CM000684.1:g.23647817G>A	GRCh37
NC_000022.9:g.21977817G>A	NCBI36
NG_009244.1:g.130266G>A
NG_009244.2:g.130266G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.3013-3794G>A MANE Select	ENSP00000303507.8:n.3013-3794G>A
ENST00000305877.12:c.3013-3794G>A	ENSP00000303507.8:n.3013-3794G>A
ENST00000359540.7:c.2881-3794G>A	ENSP00000352535.3:n.2881-3794G>A
ENST00000398512.9:c.1709-3794G>A	ENSP00000381524.6:n.1709-3794G>A
ENST00000419722.6:n.238-3794G>A
NM_004327.3:c.3013-3794G>A	NP_004318.3:n.3013-3794G>A
NM_021574.2:c.2881-3794G>A	NP_067585.2:n.2881-3794G>A
NM_004327.4:c.3013-3794G>A MANE Select	NP_004318.3:n.3013-3794G>A
NM_021574.3:c.2881-3794G>A	NP_067585.2:n.2881-3794G>A