Canonical Allele Identifier: CA513343160

Gene: BCR

Linked Data

• MyVariant Identifiers: chr22:g.23627289A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23285102A>G , CM000684.2:g.23285102A>G	GRCh38
NC_000022.10:g.23627289A>G , CM000684.1:g.23627289A>G	GRCh37
NC_000022.9:g.21957289A>G	NCBI36
NG_009244.1:g.109738A>G
NG_009244.2:g.109738A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.2307A>G MANE Select	ENSP00000303507.8:p.Glu769=
ENST00000305877.12:c.2307A>G	ENSP00000303507.8:p.Glu769=
ENST00000359540.7:c.2307A>G	ENSP00000352535.3:p.Glu769=
ENST00000398512.9:c.1270-3042A>G	ENSP00000381524.6:n.1270-3042A>G
ENST00000427791.1:c.759A>G	ENSP00000396531.1:p.Glu253=
ENST00000466076.1:n.381A>G
ENST00000487968.5:n.960A>G
NM_004327.3:c.2307A>G	NP_004318.3:p.Glu769=
NM_021574.2:c.2307A>G	NP_067585.2:p.Glu769=
NM_004327.4:c.2307A>G MANE Select	NP_004318.3:p.Glu769=
NM_021574.3:c.2307A>G	NP_067585.2:p.Glu769=