Canonical Allele Identifier: CA410896902
Gene: BCR HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.23627323G>C (hg19) chr22:g.23285136G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23285136G>C , CM000684.2:g.23285136G>C GRCh38
NC_000022.10:g.23627323G>C , CM000684.1:g.23627323G>C GRCh37
NC_000022.9:g.21957323G>C NCBI36
NG_009244.1:g.109772G>C
NG_009244.2:g.109772G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000305877.13:c.2341G>C MANE Select ENSP00000303507.8:p.Asp781His
ENST00000305877.12:c.2341G>C ENSP00000303507.8:p.Asp781His
ENST00000359540.7:c.2341G>C ENSP00000352535.3:p.Asp781His
ENST00000398512.9:c.1270-3008G>C ENSP00000381524.6:n.1270-3008G>C
ENST00000466076.1:n.415G>C
ENST00000487968.5:n.994G>C
NM_004327.3:c.2341G>C NP_004318.3:p.Asp781His
NM_021574.2:c.2341G>C NP_067585.2:p.Asp781His
NM_004327.4:c.2341G>C MANE Select NP_004318.3:p.Asp781His
NM_021574.3:c.2341G>C NP_067585.2:p.Asp781His
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Search 100 bp 3'