Canonical Allele Identifier: CA2397714809
Gene: BCR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23285087C= , CM000684.2:g.23285087C= GRCh38
NC_000022.10:g.23627274C= , CM000684.1:g.23627274C= GRCh37
NC_000022.9:g.21957274C= NCBI36
NG_009244.1:g.109723C=
NG_009244.2:g.109723C=

Transcript Alleles

HGVS Amino-acid change
ENST00000305877.13:c.2292C= MANE Select ENSP00000303507.8:p.Phe764=
ENST00000305877.12:c.2292C= ENSP00000303507.8:p.Phe764=
ENST00000359540.7:c.2292C= ENSP00000352535.3:p.Phe764=
ENST00000398512.9:c.1270-3057C= ENSP00000381524.6:n.1270-3057C=
ENST00000427791.1:c.744C= ENSP00000396531.1:p.Phe248=
ENST00000466076.1:n.366C=
ENST00000487968.5:n.945C=
NM_004327.3:c.2292C= NP_004318.3:p.Phe764=
NM_021574.2:c.2292C= NP_067585.2:p.Phe764=
NM_004327.4:c.2292C= MANE Select NP_004318.3:p.Phe764=
NM_021574.3:c.2292C= NP_067585.2:p.Phe764=