Canonical Allele Identifier: CA2818514192
Gene: BCR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23305835A>G , CM000684.2:g.23305835A>G GRCh38
NC_000022.10:g.23648022A>G , CM000684.1:g.23648022A>G GRCh37
NC_000022.9:g.21978022A>G NCBI36
NG_009244.1:g.130471A>G
NG_009244.2:g.130471A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000305877.13:c.3013-3589A>G MANE Select ENSP00000303507.8:n.3013-3589A>G
ENST00000305877.12:c.3013-3589A>G ENSP00000303507.8:n.3013-3589A>G
ENST00000359540.7:c.2881-3589A>G ENSP00000352535.3:n.2881-3589A>G
ENST00000398512.9:c.1709-3589A>G ENSP00000381524.6:n.1709-3589A>G
ENST00000419722.6:n.238-3589A>G
NM_004327.3:c.3013-3589A>G NP_004318.3:n.3013-3589A>G
NM_021574.2:c.2881-3589A>G NP_067585.2:n.2881-3589A>G
NM_004327.4:c.3013-3589A>G MANE Select NP_004318.3:n.3013-3589A>G
NM_021574.3:c.2881-3589A>G NP_067585.2:n.2881-3589A>G
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