Canonical Allele Identifier: CA2397726859
Gene: BCR HGNC NCBI

Linked Data

dbSNP Id: rs2073975488
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23308757A>G , CM000684.2:g.23308757A>G GRCh38
NC_000022.10:g.23650944A>G , CM000684.1:g.23650944A>G GRCh37
NC_000022.9:g.21980944A>G NCBI36
NG_009244.1:g.133393A>G
NG_009244.2:g.133393A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000305877.13:c.3013-667A>G MANE Select ENSP00000303507.8:n.3013-667A>G
ENST00000305877.12:c.3013-667A>G ENSP00000303507.8:n.3013-667A>G
ENST00000359540.7:c.2881-667A>G ENSP00000352535.3:n.2881-667A>G
ENST00000398512.9:c.1709-667A>G ENSP00000381524.6:n.1709-667A>G
ENST00000419722.6:n.238-667A>G
ENST00000475025.5:n.87-667A>G
ENST00000478978.5:n.294-667A>G
NM_004327.3:c.3013-667A>G NP_004318.3:n.3013-667A>G
NM_021574.2:c.2881-667A>G NP_067585.2:n.2881-667A>G
NM_004327.4:c.3013-667A>G MANE Select NP_004318.3:n.3013-667A>G
NM_021574.3:c.2881-667A>G NP_067585.2:n.2881-667A>G
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