Canonical Allele Identifier: CA751751894
Gene: BCR HGNC NCBI

Linked Data

dbSNP Id: rs1389368195
gnomAD v3: 22-23203736-G-A
gnomAD v4: 22-23203736-G-A
MyVariant Identifiers: chr22:g.23545923G>A (hg19) chr22:g.23203736G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23203736G>A , CM000684.2:g.23203736G>A GRCh38
NC_000022.10:g.23545923G>A , CM000684.1:g.23545923G>A GRCh37
NC_000022.9:g.21875923G>A NCBI36
NG_009244.1:g.28372G>A
NG_009244.2:g.28372G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000305877.13:c.1279+21497G>A MANE Select ENSP00000303507.8:n.1279+21497G>A
ENST00000305877.12:c.1279+21497G>A ENSP00000303507.8:n.1279+21497G>A
ENST00000359540.7:c.1279+21497G>A ENSP00000352535.3:n.1279+21497G>A
ENST00000398512.9:c.1269+21507G>A ENSP00000381524.6:n.1269+21507G>A
ENST00000463770.5:n.133+5351G>A
ENST00000479188.5:n.129+23904G>A
ENST00000487679.1:n.196+4384G>A
NM_004327.3:c.1279+21497G>A NP_004318.3:n.1279+21497G>A
NM_021574.2:c.1279+21497G>A NP_067585.2:n.1279+21497G>A
NM_004327.4:c.1279+21497G>A MANE Select NP_004318.3:n.1279+21497G>A
NM_021574.3:c.1279+21497G>A NP_067585.2:n.1279+21497G>A
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