Canonical Allele Identifier: CA2655651371
Gene: BCR HGNC NCBI

Linked Data

gnomAD v4: 22-23302544-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23302544C>A , CM000684.2:g.23302544C>A GRCh38
NC_000022.10:g.23644731C>A , CM000684.1:g.23644731C>A GRCh37
NC_000022.9:g.21974731C>A NCBI36
NG_009244.1:g.127180C>A
NG_009244.2:g.127180C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000305877.13:c.3013-6880C>A MANE Select ENSP00000303507.8:n.3013-6880C>A
ENST00000305877.12:c.3013-6880C>A ENSP00000303507.8:n.3013-6880C>A
ENST00000359540.7:c.2881-6880C>A ENSP00000352535.3:n.2881-6880C>A
ENST00000398512.9:c.1709-6880C>A ENSP00000381524.6:n.1709-6880C>A
ENST00000419722.6:n.238-6880C>A
ENST00000471452.1:n.319C>A
NM_004327.3:c.3013-6880C>A NP_004318.3:n.3013-6880C>A
NM_021574.2:c.2881-6880C>A NP_067585.2:n.2881-6880C>A
NM_004327.4:c.3013-6880C>A MANE Select NP_004318.3:n.3013-6880C>A
NM_021574.3:c.2881-6880C>A NP_067585.2:n.2881-6880C>A
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