Canonical Allele Identifier: CA638663560

Gene: BCR

Linked Data

• dbSNP Id: rs1314853955
• gnomAD v2: 22-23545850-A-C
• gnomAD v3: 22-23203663-A-C
• gnomAD v4: 22-23203663-A-C
• MyVariant Identifiers: chr22:g.23545850A>C (hg19) ; chr22:g.23203663A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23203663A>C , CM000684.2:g.23203663A>C	GRCh38
NC_000022.10:g.23545850A>C , CM000684.1:g.23545850A>C	GRCh37
NC_000022.9:g.21875850A>C	NCBI36
NG_009244.1:g.28299A>C
NG_009244.2:g.28299A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000305877.13:c.1279+21424A>C MANE Select	ENSP00000303507.8:n.1279+21424A>C
ENST00000305877.12:c.1279+21424A>C	ENSP00000303507.8:n.1279+21424A>C
ENST00000359540.7:c.1279+21424A>C	ENSP00000352535.3:n.1279+21424A>C
ENST00000398512.9:c.1269+21434A>C	ENSP00000381524.6:n.1269+21434A>C
ENST00000463770.5:n.133+5278A>C
ENST00000479188.5:n.129+23831A>C
ENST00000487679.1:n.196+4311A>C
NM_004327.3:c.1279+21424A>C	NP_004318.3:n.1279+21424A>C
NM_021574.2:c.1279+21424A>C	NP_067585.2:n.1279+21424A>C
NM_004327.4:c.1279+21424A>C MANE Select	NP_004318.3:n.1279+21424A>C
NM_021574.3:c.1279+21424A>C	NP_067585.2:n.1279+21424A>C