Canonical Allele Identifier: CA10142544

Gene: BCR

Linked Data

• dbSNP Id: rs747930520
• ExAC: 22:23627206 C / G
• gnomAD v2: 22-23627206-C-G
• gnomAD v4: 22-23285019-C-G
• MyVariant Identifiers: chr22:g.23627206C>G (hg19) ; chr22:g.23285019C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23285019C>G , CM000684.2:g.23285019C>G	GRCh38
NC_000022.10:g.23627206C>G , CM000684.1:g.23627206C>G	GRCh37
NC_000022.9:g.21957206C>G	NCBI36
NG_009244.1:g.109655C>G
NG_009244.2:g.109655C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.2238-14C>G MANE Select	ENSP00000303507.8:n.2238-14C>G
ENST00000305877.12:c.2238-14C>G	ENSP00000303507.8:n.2238-14C>G
ENST00000359540.7:c.2238-14C>G	ENSP00000352535.3:n.2238-14C>G
ENST00000398512.9:c.1270-3125C>G	ENSP00000381524.6:n.1270-3125C>G
ENST00000427791.1:c.690-14C>G	ENSP00000396531.1:n.690-14C>G
ENST00000466076.1:n.312-14C>G
ENST00000487968.5:n.891-14C>G
NM_004327.3:c.2238-14C>G	NP_004318.3:n.2238-14C>G
NM_021574.2:c.2238-14C>G	NP_067585.2:n.2238-14C>G
NM_004327.4:c.2238-14C>G MANE Select	NP_004318.3:n.2238-14C>G
NM_021574.3:c.2238-14C>G	NP_067585.2:n.2238-14C>G