Canonical Allele Identifier: CA2397669353

Gene: BCR

Genomic Alleles

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

Transcript Alleles

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