Canonical Allele Identifier: CA2655647378

Gene: BCR

Linked Data

• gnomAD v4: 22-23285210-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23285210C>G , CM000684.2:g.23285210C>G	GRCh38
NC_000022.10:g.23627397C>G , CM000684.1:g.23627397C>G	GRCh37
NC_000022.9:g.21957397C>G	NCBI36
NG_009244.1:g.109846C>G
NG_009244.2:g.109846C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.2406+9C>G MANE Select	ENSP00000303507.8:n.2406+9C>G
ENST00000305877.12:c.2406+9C>G	ENSP00000303507.8:n.2406+9C>G
ENST00000359540.7:c.2406+9C>G	ENSP00000352535.3:n.2406+9C>G
ENST00000398512.9:c.1270-2934C>G	ENSP00000381524.6:n.1270-2934C>G
ENST00000466076.1:n.480+9C>G
ENST00000487968.5:n.1059+9C>G
NM_004327.3:c.2406+9C>G	NP_004318.3:n.2406+9C>G
NM_021574.2:c.2406+9C>G	NP_067585.2:n.2406+9C>G
XR_001755448.1:n.1128G>C
NM_004327.4:c.2406+9C>G MANE Select	NP_004318.3:n.2406+9C>G
NM_021574.3:c.2406+9C>G	NP_067585.2:n.2406+9C>G