Canonical Allele Identifier: CA751758752

Gene: BCR

Linked Data

• dbSNP Id: rs1337797859
• gnomAD v3: 22-23216392-A-G
• gnomAD v4: 22-23216392-A-G
• MyVariant Identifiers: chr22:g.23558579A>G (hg19) ; chr22:g.23216392A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23216392A>G , CM000684.2:g.23216392A>G	GRCh38
NC_000022.10:g.23558579A>G , CM000684.1:g.23558579A>G	GRCh37
NC_000022.9:g.21888579A>G	NCBI36
NG_009244.1:g.41028A>G
NG_009244.2:g.41028A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.1279+34153A>G MANE Select	ENSP00000303507.8:n.1279+34153A>G
ENST00000305877.12:c.1279+34153A>G	ENSP00000303507.8:n.1279+34153A>G
ENST00000359540.7:c.1279+34153A>G	ENSP00000352535.3:n.1279+34153A>G
ENST00000398512.9:c.1269+34163A>G	ENSP00000381524.6:n.1269+34163A>G
ENST00000463770.5:n.133+18007A>G
ENST00000479188.5:n.130-26426A>G
ENST00000487679.1:n.196+17040A>G
NM_004327.3:c.1279+34153A>G	NP_004318.3:n.1279+34153A>G
NM_021574.2:c.1279+34153A>G	NP_067585.2:n.1279+34153A>G
NM_004327.4:c.1279+34153A>G MANE Select	NP_004318.3:n.1279+34153A>G
NM_021574.3:c.1279+34153A>G	NP_067585.2:n.1279+34153A>G