Canonical Allele Identifier: CA14987856
Gene: BCR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23305822G>A , CM000684.2:g.23305822G>A GRCh38
NC_000022.10:g.23648009G>A , CM000684.1:g.23648009G>A GRCh37
NC_000022.9:g.21978009G>A NCBI36
NG_009244.1:g.130458G>A
NG_009244.2:g.130458G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000305877.13:c.3013-3602G>A MANE Select ENSP00000303507.8:n.3013-3602G>A
ENST00000305877.12:c.3013-3602G>A ENSP00000303507.8:n.3013-3602G>A
ENST00000359540.7:c.2881-3602G>A ENSP00000352535.3:n.2881-3602G>A
ENST00000398512.9:c.1709-3602G>A ENSP00000381524.6:n.1709-3602G>A
ENST00000419722.6:n.238-3602G>A
NM_004327.3:c.3013-3602G>A NP_004318.3:n.3013-3602G>A
NM_021574.2:c.2881-3602G>A NP_067585.2:n.2881-3602G>A
NM_004327.4:c.3013-3602G>A MANE Select NP_004318.3:n.3013-3602G>A
NM_021574.3:c.2881-3602G>A NP_067585.2:n.2881-3602G>A
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