Canonical Allele Identifier: CA751751911

Gene: BCR

Linked Data

• dbSNP Id: rs1343578198
• MyVariant Identifiers: chr22:g.23545981C>T (hg19) ; chr22:g.23203794C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23203794C>T , CM000684.2:g.23203794C>T	GRCh38
NC_000022.10:g.23545981C>T , CM000684.1:g.23545981C>T	GRCh37
NC_000022.9:g.21875981C>T	NCBI36
NG_009244.1:g.28430C>T
NG_009244.2:g.28430C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.1279+21555C>T MANE Select	ENSP00000303507.8:n.1279+21555C>T
ENST00000305877.12:c.1279+21555C>T	ENSP00000303507.8:n.1279+21555C>T
ENST00000359540.7:c.1279+21555C>T	ENSP00000352535.3:n.1279+21555C>T
ENST00000398512.9:c.1269+21565C>T	ENSP00000381524.6:n.1269+21565C>T
ENST00000463770.5:n.133+5409C>T
ENST00000479188.5:n.129+23962C>T
ENST00000487679.1:n.196+4442C>T
NM_004327.3:c.1279+21555C>T	NP_004318.3:n.1279+21555C>T
NM_021574.2:c.1279+21555C>T	NP_067585.2:n.1279+21555C>T
NM_004327.4:c.1279+21555C>T MANE Select	NP_004318.3:n.1279+21555C>T
NM_021574.3:c.1279+21555C>T	NP_067585.2:n.1279+21555C>T