Canonical Allele Identifier: CA10142573
Gene: BCR HGNC NCBI

Linked Data

dbSNP Id: rs766833739

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23285193A>G , CM000684.2:g.23285193A>G GRCh38
NC_000022.10:g.23627380A>G , CM000684.1:g.23627380A>G GRCh37
NC_000022.9:g.21957380A>G NCBI36
NG_009244.1:g.109829A>G
NG_009244.2:g.109829A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000305877.13:c.2398A>G MANE Select ENSP00000303507.8:p.Arg800Gly
ENST00000305877.12:c.2398A>G ENSP00000303507.8:p.Arg800Gly
ENST00000359540.7:c.2398A>G ENSP00000352535.3:p.Arg800Gly
ENST00000398512.9:c.1270-2951A>G ENSP00000381524.6:n.1270-2951A>G
ENST00000466076.1:n.472A>G
ENST00000487968.5:n.1051A>G
NM_004327.3:c.2398A>G NP_004318.3:p.Arg800Gly
NM_021574.2:c.2398A>G NP_067585.2:p.Arg800Gly
NM_004327.4:c.2398A>G MANE Select NP_004318.3:p.Arg800Gly
NM_021574.3:c.2398A>G NP_067585.2:p.Arg800Gly