Canonical Allele Identifier: CA2397674377
Gene: BCR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23203735A= , CM000684.2:g.23203735A= GRCh38
NC_000022.10:g.23545922A= , CM000684.1:g.23545922A= GRCh37
NC_000022.9:g.21875922A= NCBI36
NG_009244.1:g.28371A=
NG_009244.2:g.28371A=

Transcript Alleles

HGVS Amino-acid change
ENST00000305877.13:c.1279+21496A= MANE Select ENSP00000303507.8:n.1279+21496A=
ENST00000305877.12:c.1279+21496A= ENSP00000303507.8:n.1279+21496A=
ENST00000359540.7:c.1279+21496A= ENSP00000352535.3:n.1279+21496A=
ENST00000398512.9:c.1269+21506A= ENSP00000381524.6:n.1269+21506A=
ENST00000463770.5:n.133+5350A=
ENST00000479188.5:n.129+23903A=
ENST00000487679.1:n.196+4383A=
NM_004327.3:c.1279+21496A= NP_004318.3:n.1279+21496A=
NM_021574.2:c.1279+21496A= NP_067585.2:n.1279+21496A=
NM_004327.4:c.1279+21496A= MANE Select NP_004318.3:n.1279+21496A=
NM_021574.3:c.1279+21496A= NP_067585.2:n.1279+21496A=