Canonical Allele Identifier: CA1645781072

Gene: BACH2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.90170676A= , CM000668.2:g.90170676A=	GRCh38
NC_000006.11:g.90880395A= , CM000668.1:g.90880395A=	GRCh37
NC_000006.10:g.90937116A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000406998.7:c.-162+35893T=	ENSP00000384145.3:n.-162+35893T=
ENST00000453877.6:c.-162+35893T=	ENSP00000397668.2:n.-162+35893T=
ENST00000470301.6:n.469+35893T=
ENST00000695952.1:c.-242+35893T=	ENSP00000512284.1:n.-242+35893T=
ENST00000695953.1:n.474+35893T=
ENST00000257749.9:c.-162+35893T= MANE Select	ENSP00000257749.4:n.-162+35893T=
ENST00000257749.8:c.-162+35893T=	ENSP00000257749.4:n.-162+35893T=
ENST00000343122.7:c.-162+35893T=	ENSP00000345642.3:n.-162+35893T=
ENST00000406998.6:c.-162+35893T=	ENSP00000384145.2:n.-162+35893T=
ENST00000453877.5:c.-162+35893T=	ENSP00000397668.1:n.-162+35893T=
ENST00000470301.5:n.469+35893T=
ENST00000472023.5:n.454+35893T=
ENST00000493201.5:n.380+35893T=
ENST00000494747.2:n.469+35893T=
ENST00000537989.5:c.-162+35893T=	ENSP00000437473.1:n.-162+35893T=
NM_001170794.1:c.-162+35893T=	NP_001164265.1:n.-162+35893T=
NM_021813.3:c.-162+35893T=	NP_068585.1:n.-162+35893T=
XM_011536037.1:c.-162+35893T=	XP_011534339.1:n.-162+35893T=
XM_011536038.1:c.-242+35893T=	XP_011534340.1:n.-242+35893T=
XM_011536039.1:c.-162+35893T=	XP_011534341.1:n.-162+35893T=
XM_011536040.1:c.-162+35893T=	XP_011534342.1:n.-162+35893T=
XM_011536041.1:c.-162+35893T=	XP_011534343.1:n.-162+35893T=
XM_011536042.1:c.65+2910T=	XP_011534344.1:n.65+2910T=
XM_011536043.1:c.65+2910T=	XP_011534345.1:n.65+2910T=
XM_011536039.3:c.-162+35893T=	XP_011534341.1:n.-162+35893T=
XM_011536040.2:c.-162+35893T=	XP_011534342.1:n.-162+35893T=
XM_017011166.2:c.-242+35893T=	XP_016866655.1:n.-242+35893T=
XM_017011167.2:c.-872+35893T=	XP_016866656.1:n.-872+35893T=
XM_024446513.1:c.-162+35893T=	XP_024302281.1:n.-162+35893T=
NM_021813.4:c.-162+35893T= MANE Select	NP_068585.1:n.-162+35893T=
NM_001170794.2:c.-162+35893T=	NP_001164265.1:n.-162+35893T=