Canonical Allele Identifier: CA410897012
Gene: BCR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23285167T>G , CM000684.2:g.23285167T>G GRCh38
NC_000022.10:g.23627354T>G , CM000684.1:g.23627354T>G GRCh37
NC_000022.9:g.21957354T>G NCBI36
NG_009244.1:g.109803T>G
NG_009244.2:g.109803T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000305877.13:c.2372T>G MANE Select ENSP00000303507.8:p.Ile791Ser
ENST00000305877.12:c.2372T>G ENSP00000303507.8:p.Ile791Ser
ENST00000359540.7:c.2372T>G ENSP00000352535.3:p.Ile791Ser
ENST00000398512.9:c.1270-2977T>G ENSP00000381524.6:n.1270-2977T>G
ENST00000466076.1:n.446T>G
ENST00000487968.5:n.1025T>G
NM_004327.3:c.2372T>G NP_004318.3:p.Ile791Ser
NM_021574.2:c.2372T>G NP_067585.2:p.Ile791Ser
NM_004327.4:c.2372T>G MANE Select NP_004318.3:p.Ile791Ser
NM_021574.3:c.2372T>G NP_067585.2:p.Ile791Ser