Canonical Allele Identifier: CA410896967
Gene: BCR HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.23627342T>A (hg19) chr22:g.23285155T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23285155T>A , CM000684.2:g.23285155T>A GRCh38
NC_000022.10:g.23627342T>A , CM000684.1:g.23627342T>A GRCh37
NC_000022.9:g.21957342T>A NCBI36
NG_009244.1:g.109791T>A
NG_009244.2:g.109791T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000305877.13:c.2360T>A MANE Select ENSP00000303507.8:p.Leu787Ter
ENST00000305877.12:c.2360T>A ENSP00000303507.8:p.Leu787Ter
ENST00000359540.7:c.2360T>A ENSP00000352535.3:p.Leu787Ter
ENST00000398512.9:c.1270-2989T>A ENSP00000381524.6:n.1270-2989T>A
ENST00000466076.1:n.434T>A
ENST00000487968.5:n.1013T>A
NM_004327.3:c.2360T>A NP_004318.3:p.Leu787Ter
NM_021574.2:c.2360T>A NP_067585.2:p.Leu787Ter
NM_004327.4:c.2360T>A MANE Select NP_004318.3:p.Leu787Ter
NM_021574.3:c.2360T>A NP_067585.2:p.Leu787Ter
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