Canonical Allele Identifier: CA2397714849
Gene: BCR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23285189C= , CM000684.2:g.23285189C= GRCh38
NC_000022.10:g.23627376C= , CM000684.1:g.23627376C= GRCh37
NC_000022.9:g.21957376C= NCBI36
NG_009244.1:g.109825C=
NG_009244.2:g.109825C=

Transcript Alleles

HGVS Amino-acid change
ENST00000305877.13:c.2394C= MANE Select ENSP00000303507.8:p.Ile798=
ENST00000305877.12:c.2394C= ENSP00000303507.8:p.Ile798=
ENST00000359540.7:c.2394C= ENSP00000352535.3:p.Ile798=
ENST00000398512.9:c.1270-2955C= ENSP00000381524.6:n.1270-2955C=
ENST00000466076.1:n.468C=
ENST00000487968.5:n.1047C=
NM_004327.3:c.2394C= NP_004318.3:p.Ile798=
NM_021574.2:c.2394C= NP_067585.2:p.Ile798=
NM_004327.4:c.2394C= MANE Select NP_004318.3:p.Ile798=
NM_021574.3:c.2394C= NP_067585.2:p.Ile798=