Canonical Allele Identifier: CA410896760

Gene: BCR

Linked Data

• MyVariant Identifiers: chr22:g.23627279T>C (hg19) ; chr22:g.23285092T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23285092T>C , CM000684.2:g.23285092T>C	GRCh38
NC_000022.10:g.23627279T>C , CM000684.1:g.23627279T>C	GRCh37
NC_000022.9:g.21957279T>C	NCBI36
NG_009244.1:g.109728T>C
NG_009244.2:g.109728T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000305877.13:c.2297T>C MANE Select	ENSP00000303507.8:p.Met766Thr
ENST00000305877.12:c.2297T>C	ENSP00000303507.8:p.Met766Thr
ENST00000359540.7:c.2297T>C	ENSP00000352535.3:p.Met766Thr
ENST00000398512.9:c.1270-3052T>C	ENSP00000381524.6:n.1270-3052T>C
ENST00000427791.1:c.749T>C	ENSP00000396531.1:p.Met250Thr
ENST00000466076.1:n.371T>C
ENST00000487968.5:n.950T>C
NM_004327.3:c.2297T>C	NP_004318.3:p.Met766Thr
NM_021574.2:c.2297T>C	NP_067585.2:p.Met766Thr
NM_004327.4:c.2297T>C MANE Select	NP_004318.3:p.Met766Thr
NM_021574.3:c.2297T>C	NP_067585.2:p.Met766Thr