Canonical Allele Identifier: CA2397714813
Gene: BCR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23285093G= , CM000684.2:g.23285093G= GRCh38
NC_000022.10:g.23627280G= , CM000684.1:g.23627280G= GRCh37
NC_000022.9:g.21957280G= NCBI36
NG_009244.1:g.109729G=
NG_009244.2:g.109729G=

Transcript Alleles

HGVS Amino-acid change
ENST00000305877.13:c.2298G= MANE Select ENSP00000303507.8:p.Met766=
ENST00000305877.12:c.2298G= ENSP00000303507.8:p.Met766=
ENST00000359540.7:c.2298G= ENSP00000352535.3:p.Met766=
ENST00000398512.9:c.1270-3051G= ENSP00000381524.6:n.1270-3051G=
ENST00000427791.1:c.750G= ENSP00000396531.1:p.Met250=
ENST00000466076.1:n.372G=
ENST00000487968.5:n.951G=
NM_004327.3:c.2298G= NP_004318.3:p.Met766=
NM_021574.2:c.2298G= NP_067585.2:p.Met766=
NM_004327.4:c.2298G= MANE Select NP_004318.3:p.Met766=
NM_021574.3:c.2298G= NP_067585.2:p.Met766=