Canonical Allele Identifier: CA410896769

Gene: BCR

Linked Data

• dbSNP Id: rs1401998291
• gnomAD v2: 22-23627281-G-A
• gnomAD v4: 22-23285094-G-A
• MyVariant Identifiers: chr22:g.23627281G>A (hg19) ; chr22:g.23285094G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23285094G>A , CM000684.2:g.23285094G>A	GRCh38
NC_000022.10:g.23627281G>A , CM000684.1:g.23627281G>A	GRCh37
NC_000022.9:g.21957281G>A	NCBI36
NG_009244.1:g.109730G>A
NG_009244.2:g.109730G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.2299G>A MANE Select	ENSP00000303507.8:p.Val767Met
ENST00000305877.12:c.2299G>A	ENSP00000303507.8:p.Val767Met
ENST00000359540.7:c.2299G>A	ENSP00000352535.3:p.Val767Met
ENST00000398512.9:c.1270-3050G>A	ENSP00000381524.6:n.1270-3050G>A
ENST00000427791.1:c.751G>A	ENSP00000396531.1:p.Val251Met
ENST00000466076.1:n.373G>A
ENST00000487968.5:n.952G>A
NM_004327.3:c.2299G>A	NP_004318.3:p.Val767Met
NM_021574.2:c.2299G>A	NP_067585.2:p.Val767Met
NM_004327.4:c.2299G>A MANE Select	NP_004318.3:p.Val767Met
NM_021574.3:c.2299G>A	NP_067585.2:p.Val767Met