Canonical Allele Identifier: CA410897132
Gene: BCR HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.23627385G>C (hg19) chr22:g.23285198G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23285198G>C , CM000684.2:g.23285198G>C GRCh38
NC_000022.10:g.23627385G>C , CM000684.1:g.23627385G>C GRCh37
NC_000022.9:g.21957385G>C NCBI36
NG_009244.1:g.109834G>C
NG_009244.2:g.109834G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000305877.13:c.2403G>C MANE Select ENSP00000303507.8:p.Glu801Asp
ENST00000305877.12:c.2403G>C ENSP00000303507.8:p.Glu801Asp
ENST00000359540.7:c.2403G>C ENSP00000352535.3:p.Glu801Asp
ENST00000398512.9:c.1270-2946G>C ENSP00000381524.6:n.1270-2946G>C
ENST00000466076.1:n.477G>C
ENST00000487968.5:n.1056G>C
NM_004327.3:c.2403G>C NP_004318.3:p.Glu801Asp
NM_021574.2:c.2403G>C NP_067585.2:p.Glu801Asp
NM_004327.4:c.2403G>C MANE Select NP_004318.3:p.Glu801Asp
NM_021574.3:c.2403G>C NP_067585.2:p.Glu801Asp
Search 100 bp 5'
Search 100 bp 3'