Canonical Allele Identifier: CA322517156

Gene: BCR

Linked Data

• dbSNP Id: rs922454997
• gnomAD v3: 22-23305908-C-T
• gnomAD v4: 22-23305908-C-T
• MyVariant Identifiers: chr22:g.23648095C>T (hg19) ; chr22:g.23305908C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23305908C>T , CM000684.2:g.23305908C>T	GRCh38
NC_000022.10:g.23648095C>T , CM000684.1:g.23648095C>T	GRCh37
NC_000022.9:g.21978095C>T	NCBI36
NG_009244.1:g.130544C>T
NG_009244.2:g.130544C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.3013-3516C>T MANE Select	ENSP00000303507.8:n.3013-3516C>T
ENST00000305877.12:c.3013-3516C>T	ENSP00000303507.8:n.3013-3516C>T
ENST00000359540.7:c.2881-3516C>T	ENSP00000352535.3:n.2881-3516C>T
ENST00000398512.9:c.1709-3516C>T	ENSP00000381524.6:n.1709-3516C>T
ENST00000419722.6:n.238-3516C>T
NM_004327.3:c.3013-3516C>T	NP_004318.3:n.3013-3516C>T
NM_021574.2:c.2881-3516C>T	NP_067585.2:n.2881-3516C>T
NM_004327.4:c.3013-3516C>T MANE Select	NP_004318.3:n.3013-3516C>T
NM_021574.3:c.2881-3516C>T	NP_067585.2:n.2881-3516C>T