Canonical Allele Identifier: CA2397669351

Gene: BCR

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23193795G>C , CM000684.2:g.23193795G>C	GRCh38
NC_000022.10:g.23535982G>C , CM000684.1:g.23535982G>C	GRCh37
NC_000022.9:g.21865982G>C	NCBI36
NG_009244.1:g.18431G>C
NG_009244.2:g.18431G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.1279+11556G>C MANE Select	ENSP00000303507.8:n.1279+11556G>C
ENST00000305877.12:c.1279+11556G>C	ENSP00000303507.8:n.1279+11556G>C
ENST00000359540.7:c.1279+11556G>C	ENSP00000352535.3:n.1279+11556G>C
ENST00000398512.9:c.1269+11566G>C	ENSP00000381524.6:n.1269+11566G>C
ENST00000479188.5:n.129+13963G>C
NM_004327.3:c.1279+11556G>C	NP_004318.3:n.1279+11556G>C
NM_021574.2:c.1279+11556G>C	NP_067585.2:n.1279+11556G>C
NM_004327.4:c.1279+11556G>C MANE Select	NP_004318.3:n.1279+11556G>C
NM_021574.3:c.1279+11556G>C	NP_067585.2:n.1279+11556G>C