Canonical Allele Identifier: CA751751854

Gene: BCR

Linked Data

• dbSNP Id: rs1329837230
• gnomAD v3: 22-23203690-G-A
• gnomAD v4: 22-23203690-G-A
• MyVariant Identifiers: chr22:g.23545877G>A (hg19) ; chr22:g.23203690G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23203690G>A , CM000684.2:g.23203690G>A	GRCh38
NC_000022.10:g.23545877G>A , CM000684.1:g.23545877G>A	GRCh37
NC_000022.9:g.21875877G>A	NCBI36
NG_009244.1:g.28326G>A
NG_009244.2:g.28326G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.1279+21451G>A MANE Select	ENSP00000303507.8:n.1279+21451G>A
ENST00000305877.12:c.1279+21451G>A	ENSP00000303507.8:n.1279+21451G>A
ENST00000359540.7:c.1279+21451G>A	ENSP00000352535.3:n.1279+21451G>A
ENST00000398512.9:c.1269+21461G>A	ENSP00000381524.6:n.1269+21461G>A
ENST00000463770.5:n.133+5305G>A
ENST00000479188.5:n.129+23858G>A
ENST00000487679.1:n.196+4338G>A
NM_004327.3:c.1279+21451G>A	NP_004318.3:n.1279+21451G>A
NM_021574.2:c.1279+21451G>A	NP_067585.2:n.1279+21451G>A
NM_004327.4:c.1279+21451G>A MANE Select	NP_004318.3:n.1279+21451G>A
NM_021574.3:c.1279+21451G>A	NP_067585.2:n.1279+21451G>A