Canonical Allele Identifier: CA410896758

Gene: BCR

Linked Data

• gnomAD v4: 22-23285091-A-T
• MyVariant Identifiers: chr22:g.23627278A>T (hg19) ; chr22:g.23285091A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000305877.13:c.2296A>T MANE Select	ENSP00000303507.8:p.Met766Leu
ENST00000305877.12:c.2296A>T	ENSP00000303507.8:p.Met766Leu
ENST00000359540.7:c.2296A>T	ENSP00000352535.3:p.Met766Leu
ENST00000398512.9:c.1270-3053A>T	ENSP00000381524.6:n.1270-3053A>T
ENST00000427791.1:c.748A>T	ENSP00000396531.1:p.Met250Leu
ENST00000466076.1:n.370A>T
ENST00000487968.5:n.949A>T
NM_004327.3:c.2296A>T	NP_004318.3:p.Met766Leu
NM_021574.2:c.2296A>T	NP_067585.2:p.Met766Leu
NM_004327.4:c.2296A>T MANE Select	NP_004318.3:p.Met766Leu
NM_021574.3:c.2296A>T	NP_067585.2:p.Met766Leu