Canonical Allele Identifier: CA2655651357

Gene: BCR

Linked Data

• gnomAD v4: 22-23302518-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23302518C>T , CM000684.2:g.23302518C>T	GRCh38
NC_000022.10:g.23644705C>T , CM000684.1:g.23644705C>T	GRCh37
NC_000022.9:g.21974705C>T	NCBI36
NG_009244.1:g.127154C>T
NG_009244.2:g.127154C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000305877.13:c.3013-6906C>T MANE Select	ENSP00000303507.8:n.3013-6906C>T
ENST00000305877.12:c.3013-6906C>T	ENSP00000303507.8:n.3013-6906C>T
ENST00000359540.7:c.2881-6906C>T	ENSP00000352535.3:n.2881-6906C>T
ENST00000398512.9:c.1709-6906C>T	ENSP00000381524.6:n.1709-6906C>T
ENST00000419722.6:n.238-6906C>T
ENST00000471452.1:n.293C>T
NM_004327.3:c.3013-6906C>T	NP_004318.3:n.3013-6906C>T
NM_021574.2:c.2881-6906C>T	NP_067585.2:n.2881-6906C>T
NM_004327.4:c.3013-6906C>T MANE Select	NP_004318.3:n.3013-6906C>T
NM_021574.3:c.2881-6906C>T	NP_067585.2:n.2881-6906C>T