Canonical Allele Identifier: CA322516977

Gene: BCR

Linked Data

• dbSNP Id: rs576171131
• gnomAD v2: 22-23647821-A-G
• gnomAD v3: 22-23305634-A-G
• gnomAD v4: 22-23305634-A-G
• MyVariant Identifiers: chr22:g.23647821A>G (hg19) ; chr22:g.23305634A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23305634A>G , CM000684.2:g.23305634A>G	GRCh38
NC_000022.10:g.23647821A>G , CM000684.1:g.23647821A>G	GRCh37
NC_000022.9:g.21977821A>G	NCBI36
NG_009244.1:g.130270A>G
NG_009244.2:g.130270A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000305877.13:c.3013-3790A>G MANE Select	ENSP00000303507.8:n.3013-3790A>G
ENST00000305877.12:c.3013-3790A>G	ENSP00000303507.8:n.3013-3790A>G
ENST00000359540.7:c.2881-3790A>G	ENSP00000352535.3:n.2881-3790A>G
ENST00000398512.9:c.1709-3790A>G	ENSP00000381524.6:n.1709-3790A>G
ENST00000419722.6:n.238-3790A>G
NM_004327.3:c.3013-3790A>G	NP_004318.3:n.3013-3790A>G
NM_021574.2:c.2881-3790A>G	NP_067585.2:n.2881-3790A>G
NM_004327.4:c.3013-3790A>G MANE Select	NP_004318.3:n.3013-3790A>G
NM_021574.3:c.2881-3790A>G	NP_067585.2:n.2881-3790A>G