Canonical Allele Identifier: CA322518790

Gene: BCR

Linked Data

• dbSNP Id: rs1005102322
• gnomAD v2: 22-23650897-G-A
• gnomAD v3: 22-23308710-G-A
• gnomAD v4: 22-23308710-G-A
• MyVariant Identifiers: chr22:g.23650897G>A (hg19) ; chr22:g.23308710G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23308710G>A , CM000684.2:g.23308710G>A	GRCh38
NC_000022.10:g.23650897G>A , CM000684.1:g.23650897G>A	GRCh37
NC_000022.9:g.21980897G>A	NCBI36
NG_009244.1:g.133346G>A
NG_009244.2:g.133346G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.3013-714G>A MANE Select	ENSP00000303507.8:n.3013-714G>A
ENST00000305877.12:c.3013-714G>A	ENSP00000303507.8:n.3013-714G>A
ENST00000359540.7:c.2881-714G>A	ENSP00000352535.3:n.2881-714G>A
ENST00000398512.9:c.1709-714G>A	ENSP00000381524.6:n.1709-714G>A
ENST00000419722.6:n.238-714G>A
ENST00000475025.5:n.87-714G>A
ENST00000478978.5:n.294-714G>A
NM_004327.3:c.3013-714G>A	NP_004318.3:n.3013-714G>A
NM_021574.2:c.2881-714G>A	NP_067585.2:n.2881-714G>A
NM_004327.4:c.3013-714G>A MANE Select	NP_004318.3:n.3013-714G>A
NM_021574.3:c.2881-714G>A	NP_067585.2:n.2881-714G>A