Canonical Allele Identifier: CA638664685

Gene: BCR

Linked Data

• dbSNP Id: rs1187379955
• gnomAD v2: 22-23650879-A-G
• gnomAD v3: 22-23308692-A-G
• gnomAD v4: 22-23308692-A-G
• MyVariant Identifiers: chr22:g.23650879A>G (hg19) ; chr22:g.23308692A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23308692A>G , CM000684.2:g.23308692A>G	GRCh38
NC_000022.10:g.23650879A>G , CM000684.1:g.23650879A>G	GRCh37
NC_000022.9:g.21980879A>G	NCBI36
NG_009244.1:g.133328A>G
NG_009244.2:g.133328A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.3013-732A>G MANE Select	ENSP00000303507.8:n.3013-732A>G
ENST00000305877.12:c.3013-732A>G	ENSP00000303507.8:n.3013-732A>G
ENST00000359540.7:c.2881-732A>G	ENSP00000352535.3:n.2881-732A>G
ENST00000398512.9:c.1709-732A>G	ENSP00000381524.6:n.1709-732A>G
ENST00000419722.6:n.238-732A>G
ENST00000475025.5:n.87-732A>G
ENST00000478978.5:n.294-732A>G
NM_004327.3:c.3013-732A>G	NP_004318.3:n.3013-732A>G
NM_021574.2:c.2881-732A>G	NP_067585.2:n.2881-732A>G
NM_004327.4:c.3013-732A>G MANE Select	NP_004318.3:n.3013-732A>G
NM_021574.3:c.2881-732A>G	NP_067585.2:n.2881-732A>G