Canonical Allele Identifier: CA410896854
Gene: BCR HGNC NCBI

Linked Data

dbSNP Id: rs2073696323
MyVariant Identifiers: chr22:g.23627305A>G (hg19) chr22:g.23285118A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23285118A>G , CM000684.2:g.23285118A>G GRCh38
NC_000022.10:g.23627305A>G , CM000684.1:g.23627305A>G GRCh37
NC_000022.9:g.21957305A>G NCBI36
NG_009244.1:g.109754A>G
NG_009244.2:g.109754A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000305877.13:c.2323A>G MANE Select ENSP00000303507.8:p.Asn775Asp
ENST00000305877.12:c.2323A>G ENSP00000303507.8:p.Asn775Asp
ENST00000359540.7:c.2323A>G ENSP00000352535.3:p.Asn775Asp
ENST00000398512.9:c.1270-3026A>G ENSP00000381524.6:n.1270-3026A>G
ENST00000466076.1:n.397A>G
ENST00000487968.5:n.976A>G
NM_004327.3:c.2323A>G NP_004318.3:p.Asn775Asp
NM_021574.2:c.2323A>G NP_067585.2:p.Asn775Asp
NM_004327.4:c.2323A>G MANE Select NP_004318.3:p.Asn775Asp
NM_021574.3:c.2323A>G NP_067585.2:p.Asn775Asp
Search 100 bp 5'
Search 100 bp 3'