Canonical Allele Identifier: CA410896758
Gene: BCR HGNC NCBI

Linked Data

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