Canonical Allele Identifier: CA322518666

Gene: BCR

Linked Data

• dbSNP Id: rs11705412
• MyVariant Identifiers: chr22:g.23650820C>G (hg19) ; chr22:g.23308633C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23308633C>G , CM000684.2:g.23308633C>G	GRCh38
NC_000022.10:g.23650820C>G , CM000684.1:g.23650820C>G	GRCh37
NC_000022.9:g.21980820C>G	NCBI36
NG_009244.1:g.133269C>G
NG_009244.2:g.133269C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.3013-791C>G MANE Select	ENSP00000303507.8:n.3013-791C>G
ENST00000305877.12:c.3013-791C>G	ENSP00000303507.8:n.3013-791C>G
ENST00000359540.7:c.2881-791C>G	ENSP00000352535.3:n.2881-791C>G
ENST00000398512.9:c.1709-791C>G	ENSP00000381524.6:n.1709-791C>G
ENST00000419722.6:n.238-791C>G
ENST00000475025.5:n.87-791C>G
ENST00000478978.5:n.294-791C>G
NM_004327.3:c.3013-791C>G	NP_004318.3:n.3013-791C>G
NM_021574.2:c.2881-791C>G	NP_067585.2:n.2881-791C>G
NM_004327.4:c.3013-791C>G MANE Select	NP_004318.3:n.3013-791C>G
NM_021574.3:c.2881-791C>G	NP_067585.2:n.2881-791C>G