Canonical Allele Identifier: CA322517143
Gene: BCR HGNC NCBI

Linked Data

dbSNP Id: rs1030309582
MyVariant Identifiers: chr22:g.23305876C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23305876C>T , CM000684.2:g.23305876C>T GRCh38
NC_000022.10:g.23648063C>T , CM000684.1:g.23648063C>T GRCh37
NC_000022.9:g.21978063C>T NCBI36
NG_009244.1:g.130512C>T
NG_009244.2:g.130512C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000305877.13:c.3013-3548C>T MANE Select ENSP00000303507.8:n.3013-3548C>T
ENST00000305877.12:c.3013-3548C>T ENSP00000303507.8:n.3013-3548C>T
ENST00000359540.7:c.2881-3548C>T ENSP00000352535.3:n.2881-3548C>T
ENST00000398512.9:c.1709-3548C>T ENSP00000381524.6:n.1709-3548C>T
ENST00000419722.6:n.238-3548C>T
NM_004327.3:c.3013-3548C>T NP_004318.3:n.3013-3548C>T
NM_021574.2:c.2881-3548C>T NP_067585.2:n.2881-3548C>T
NM_004327.4:c.3013-3548C>T MANE Select NP_004318.3:n.3013-3548C>T
NM_021574.3:c.2881-3548C>T NP_067585.2:n.2881-3548C>T