Canonical Allele Identifier: CA14973547
Gene: BCR HGNC NCBI

Linked Data

dbSNP Id: rs5996486

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23203756A>G , CM000684.2:g.23203756A>G GRCh38
NC_000022.10:g.23545943A>G , CM000684.1:g.23545943A>G GRCh37
NC_000022.9:g.21875943A>G NCBI36
NG_009244.1:g.28392A>G
NG_009244.2:g.28392A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000305877.13:c.1279+21517A>G MANE Select ENSP00000303507.8:n.1279+21517A>G
ENST00000305877.12:c.1279+21517A>G ENSP00000303507.8:n.1279+21517A>G
ENST00000359540.7:c.1279+21517A>G ENSP00000352535.3:n.1279+21517A>G
ENST00000398512.9:c.1269+21527A>G ENSP00000381524.6:n.1269+21527A>G
ENST00000463770.5:n.133+5371A>G
ENST00000479188.5:n.129+23924A>G
ENST00000487679.1:n.196+4404A>G
NM_004327.3:c.1279+21517A>G NP_004318.3:n.1279+21517A>G
NM_021574.2:c.1279+21517A>G NP_067585.2:n.1279+21517A>G
NM_004327.4:c.1279+21517A>G MANE Select NP_004318.3:n.1279+21517A>G
NM_021574.3:c.1279+21517A>G NP_067585.2:n.1279+21517A>G