Canonical Allele Identifier: CA2397726757
Gene: BCR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23308580C= , CM000684.2:g.23308580C= GRCh38
NC_000022.10:g.23650767C= , CM000684.1:g.23650767C= GRCh37
NC_000022.9:g.21980767C= NCBI36
NG_009244.1:g.133216C=
NG_009244.2:g.133216C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000305877.13:c.3013-844C= MANE Select ENSP00000303507.8:n.3013-844C=
ENST00000305877.12:c.3013-844C= ENSP00000303507.8:n.3013-844C=
ENST00000359540.7:c.2881-844C= ENSP00000352535.3:n.2881-844C=
ENST00000398512.9:c.1709-844C= ENSP00000381524.6:n.1709-844C=
ENST00000419722.6:n.238-844C=
ENST00000475025.5:n.87-844C=
ENST00000478978.5:n.293+816C=
NM_004327.3:c.3013-844C= NP_004318.3:n.3013-844C=
NM_021574.2:c.2881-844C= NP_067585.2:n.2881-844C=
NM_004327.4:c.3013-844C= MANE Select NP_004318.3:n.3013-844C=
NM_021574.3:c.2881-844C= NP_067585.2:n.2881-844C=
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