Canonical Allele Identifier: CA638949568

Gene: BCR

Linked Data

• dbSNP Id: rs1406337284
• gnomAD v2: 22-23627493-T-C
• gnomAD v3: 22-23285306-T-C
• gnomAD v4: 22-23285306-T-C
• MyVariant Identifiers: chr22:g.23627493T>C (hg19) ; chr22:g.23285306T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23285306T>C , CM000684.2:g.23285306T>C	GRCh38
NC_000022.10:g.23627493T>C , CM000684.1:g.23627493T>C	GRCh37
NC_000022.9:g.21957493T>C	NCBI36
NG_009244.1:g.109942T>C
NG_009244.2:g.109942T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.2406+105T>C MANE Select	ENSP00000303507.8:n.2406+105T>C
ENST00000305877.12:c.2406+105T>C	ENSP00000303507.8:n.2406+105T>C
ENST00000359540.7:c.2406+105T>C	ENSP00000352535.3:n.2406+105T>C
ENST00000398512.9:c.1270-2838T>C	ENSP00000381524.6:n.1270-2838T>C
ENST00000466076.1:n.480+105T>C
ENST00000487968.5:n.1059+105T>C
NM_004327.3:c.2406+105T>C	NP_004318.3:n.2406+105T>C
NM_021574.2:c.2406+105T>C	NP_067585.2:n.2406+105T>C
XR_001755448.1:n.1032A>G
NM_004327.4:c.2406+105T>C MANE Select	NP_004318.3:n.2406+105T>C
NM_021574.3:c.2406+105T>C	NP_067585.2:n.2406+105T>C