Canonical Allele Identifier: CA410897089

Gene: BCR

Linked Data

• MyVariant Identifiers: chr22:g.23627373C>G (hg19) ; chr22:g.23285186C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23285186C>G , CM000684.2:g.23285186C>G	GRCh38
NC_000022.10:g.23627373C>G , CM000684.1:g.23627373C>G	GRCh37
NC_000022.9:g.21957373C>G	NCBI36
NG_009244.1:g.109822C>G
NG_009244.2:g.109822C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000305877.13:c.2391C>G MANE Select	ENSP00000303507.8:p.Asp797Glu
ENST00000305877.12:c.2391C>G	ENSP00000303507.8:p.Asp797Glu
ENST00000359540.7:c.2391C>G	ENSP00000352535.3:p.Asp797Glu
ENST00000398512.9:c.1270-2958C>G	ENSP00000381524.6:n.1270-2958C>G
ENST00000466076.1:n.465C>G
ENST00000487968.5:n.1044C>G
NM_004327.3:c.2391C>G	NP_004318.3:p.Asp797Glu
NM_021574.2:c.2391C>G	NP_067585.2:p.Asp797Glu
NM_004327.4:c.2391C>G MANE Select	NP_004318.3:p.Asp797Glu
NM_021574.3:c.2391C>G	NP_067585.2:p.Asp797Glu