Canonical Allele Identifier: CA410896756

Gene: BCR

Linked Data

• MyVariant Identifiers: chr22:g.23627278A>G (hg19) ; chr22:g.23285091A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23285091A>G , CM000684.2:g.23285091A>G	GRCh38
NC_000022.10:g.23627278A>G , CM000684.1:g.23627278A>G	GRCh37
NC_000022.9:g.21957278A>G	NCBI36
NG_009244.1:g.109727A>G
NG_009244.2:g.109727A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000305877.13:c.2296A>G MANE Select	ENSP00000303507.8:p.Met766Val
ENST00000305877.12:c.2296A>G	ENSP00000303507.8:p.Met766Val
ENST00000359540.7:c.2296A>G	ENSP00000352535.3:p.Met766Val
ENST00000398512.9:c.1270-3053A>G	ENSP00000381524.6:n.1270-3053A>G
ENST00000427791.1:c.748A>G	ENSP00000396531.1:p.Met250Val
ENST00000466076.1:n.370A>G
ENST00000487968.5:n.949A>G
NM_004327.3:c.2296A>G	NP_004318.3:p.Met766Val
NM_021574.2:c.2296A>G	NP_067585.2:p.Met766Val
NM_004327.4:c.2296A>G MANE Select	NP_004318.3:p.Met766Val
NM_021574.3:c.2296A>G	NP_067585.2:p.Met766Val