Canonical Allele Identifier: CA2655651412
Gene: BCR HGNC NCBI

Linked Data

gnomAD v4: 22-23302610-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23302610A>G , CM000684.2:g.23302610A>G GRCh38
NC_000022.10:g.23644797A>G , CM000684.1:g.23644797A>G GRCh37
NC_000022.9:g.21974797A>G NCBI36
NG_009244.1:g.127246A>G
NG_009244.2:g.127246A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000305877.13:c.3013-6814A>G MANE Select ENSP00000303507.8:n.3013-6814A>G
ENST00000305877.12:c.3013-6814A>G ENSP00000303507.8:n.3013-6814A>G
ENST00000359540.7:c.2881-6814A>G ENSP00000352535.3:n.2881-6814A>G
ENST00000398512.9:c.1709-6814A>G ENSP00000381524.6:n.1709-6814A>G
ENST00000419722.6:n.238-6814A>G
ENST00000471452.1:n.385A>G
NM_004327.3:c.3013-6814A>G NP_004318.3:n.3013-6814A>G
NM_021574.2:c.2881-6814A>G NP_067585.2:n.2881-6814A>G
NM_004327.4:c.3013-6814A>G MANE Select NP_004318.3:n.3013-6814A>G
NM_021574.3:c.2881-6814A>G NP_067585.2:n.2881-6814A>G
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