Canonical Allele Identifier: CA14956513
Gene: BCR HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2267013

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23203692A>G , CM000684.2:g.23203692A>G GRCh38
NC_000022.10:g.23545879A>G , CM000684.1:g.23545879A>G GRCh37
NC_000022.9:g.21875879A>G NCBI36
NG_009244.1:g.28328A>G
NG_009244.2:g.28328A>G

Transcript Alleles

HGVS Amino-acid change
NM_004327.3:c.1279+21453A>G VV NP_004318.3:p.=
NM_021574.2:c.1279+21453A>G VV NP_067585.2:p.=
ENST00000305877.12:c.1279+21453A>G ENSP00000303507.8:p.=
ENST00000359540.7:c.1279+21453A>G ENSP00000352535.3:p.=
ENST00000398512.9:n.1269+21463A>G ENSP00000381524.6:p.=
ENST00000463770.5:n.133+5307A>G
ENST00000479188.5:n.129+23860A>G
ENST00000487679.1:n.196+4340A>G