Canonical Allele Identifier: CA2397725414
Gene: BCR HGNC NCBI

Linked Data

dbSNP Id: rs1602128085
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23305812C>G , CM000684.2:g.23305812C>G GRCh38
NC_000022.10:g.23647999C>G , CM000684.1:g.23647999C>G GRCh37
NC_000022.9:g.21977999C>G NCBI36
NG_009244.1:g.130448C>G
NG_009244.2:g.130448C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000305877.13:c.3013-3612C>G MANE Select ENSP00000303507.8:n.3013-3612C>G
ENST00000305877.12:c.3013-3612C>G ENSP00000303507.8:n.3013-3612C>G
ENST00000359540.7:c.2881-3612C>G ENSP00000352535.3:n.2881-3612C>G
ENST00000398512.9:c.1709-3612C>G ENSP00000381524.6:n.1709-3612C>G
ENST00000419722.6:n.238-3612C>G
NM_004327.3:c.3013-3612C>G NP_004318.3:n.3013-3612C>G
NM_021574.2:c.2881-3612C>G NP_067585.2:n.2881-3612C>G
NM_004327.4:c.3013-3612C>G MANE Select NP_004318.3:n.3013-3612C>G
NM_021574.3:c.2881-3612C>G NP_067585.2:n.2881-3612C>G
Search 100 bp 5'
Search 100 bp 3'