Canonical Allele Identifier: CA751769447

Gene: BCR

Linked Data

• dbSNP Id: rs1185620290
• gnomAD v3: 22-23308731-T-C
• gnomAD v4: 22-23308731-T-C
• MyVariant Identifiers: chr22:g.23650918T>C (hg19) ; chr22:g.23308731T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23308731T>C , CM000684.2:g.23308731T>C	GRCh38
NC_000022.10:g.23650918T>C , CM000684.1:g.23650918T>C	GRCh37
NC_000022.9:g.21980918T>C	NCBI36
NG_009244.1:g.133367T>C
NG_009244.2:g.133367T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.3013-693T>C MANE Select	ENSP00000303507.8:n.3013-693T>C
ENST00000305877.12:c.3013-693T>C	ENSP00000303507.8:n.3013-693T>C
ENST00000359540.7:c.2881-693T>C	ENSP00000352535.3:n.2881-693T>C
ENST00000398512.9:c.1709-693T>C	ENSP00000381524.6:n.1709-693T>C
ENST00000419722.6:n.238-693T>C
ENST00000475025.5:n.87-693T>C
ENST00000478978.5:n.294-693T>C
NM_004327.3:c.3013-693T>C	NP_004318.3:n.3013-693T>C
NM_021574.2:c.2881-693T>C	NP_067585.2:n.2881-693T>C
NM_004327.4:c.3013-693T>C MANE Select	NP_004318.3:n.3013-693T>C
NM_021574.3:c.2881-693T>C	NP_067585.2:n.2881-693T>C