Canonical Allele Identifier: CA10142569

Gene: BCR

Linked Data

• dbSNP Id: rs761957590
• ExAC: 22:23627353 A / G
• gnomAD v2: 22-23627353-A-G
• gnomAD v4: 22-23285166-A-G
• MyVariant Identifiers: chr22:g.23627353A>G (hg19) ; chr22:g.23285166A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23285166A>G , CM000684.2:g.23285166A>G	GRCh38
NC_000022.10:g.23627353A>G , CM000684.1:g.23627353A>G	GRCh37
NC_000022.9:g.21957353A>G	NCBI36
NG_009244.1:g.109802A>G
NG_009244.2:g.109802A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.2371A>G MANE Select	ENSP00000303507.8:p.Ile791Val
ENST00000305877.12:c.2371A>G	ENSP00000303507.8:p.Ile791Val
ENST00000359540.7:c.2371A>G	ENSP00000352535.3:p.Ile791Val
ENST00000398512.9:c.1270-2978A>G	ENSP00000381524.6:n.1270-2978A>G
ENST00000466076.1:n.445A>G
ENST00000487968.5:n.1024A>G
NM_004327.3:c.2371A>G	NP_004318.3:p.Ile791Val
NM_021574.2:c.2371A>G	NP_067585.2:p.Ile791Val
NM_004327.4:c.2371A>G MANE Select	NP_004318.3:p.Ile791Val
NM_021574.3:c.2371A>G	NP_067585.2:p.Ile791Val