Canonical Allele Identifier: CA2655647379

Gene: BCR

Linked Data

• gnomAD v4: 22-23285212-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23285212G>T , CM000684.2:g.23285212G>T	GRCh38
NC_000022.10:g.23627399G>T , CM000684.1:g.23627399G>T	GRCh37
NC_000022.9:g.21957399G>T	NCBI36
NG_009244.1:g.109848G>T
NG_009244.2:g.109848G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000305877.13:c.2406+11G>T MANE Select	ENSP00000303507.8:n.2406+11G>T
ENST00000305877.12:c.2406+11G>T	ENSP00000303507.8:n.2406+11G>T
ENST00000359540.7:c.2406+11G>T	ENSP00000352535.3:n.2406+11G>T
ENST00000398512.9:c.1270-2932G>T	ENSP00000381524.6:n.1270-2932G>T
ENST00000466076.1:n.480+11G>T
ENST00000487968.5:n.1059+11G>T
NM_004327.3:c.2406+11G>T	NP_004318.3:n.2406+11G>T
NM_021574.2:c.2406+11G>T	NP_067585.2:n.2406+11G>T
XR_001755448.1:n.1126C>A
NM_004327.4:c.2406+11G>T MANE Select	NP_004318.3:n.2406+11G>T
NM_021574.3:c.2406+11G>T	NP_067585.2:n.2406+11G>T