Canonical Allele Identifier: CA2655647442

Gene: BCR

Linked Data

• gnomAD v4: 22-23285286-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23285286T>C , CM000684.2:g.23285286T>C	GRCh38
NC_000022.10:g.23627473T>C , CM000684.1:g.23627473T>C	GRCh37
NC_000022.9:g.21957473T>C	NCBI36
NG_009244.1:g.109922T>C
NG_009244.2:g.109922T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.2406+85T>C MANE Select	ENSP00000303507.8:n.2406+85T>C
ENST00000305877.12:c.2406+85T>C	ENSP00000303507.8:n.2406+85T>C
ENST00000359540.7:c.2406+85T>C	ENSP00000352535.3:n.2406+85T>C
ENST00000398512.9:c.1270-2858T>C	ENSP00000381524.6:n.1270-2858T>C
ENST00000466076.1:n.480+85T>C
ENST00000487968.5:n.1059+85T>C
NM_004327.3:c.2406+85T>C	NP_004318.3:n.2406+85T>C
NM_021574.2:c.2406+85T>C	NP_067585.2:n.2406+85T>C
XR_001755448.1:n.1052A>G
NM_004327.4:c.2406+85T>C MANE Select	NP_004318.3:n.2406+85T>C
NM_021574.3:c.2406+85T>C	NP_067585.2:n.2406+85T>C