Canonical Allele Identifier: CA1645809271

Gene: BACH2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.90247744C= , CM000668.2:g.90247744C=	GRCh38
NC_000006.11:g.90957463C= , CM000668.1:g.90957463C=	GRCh37
NC_000006.10:g.91014184C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_021813.4:c.-275+4769G= MANE Select	NP_068585.1:n.-275+4769G=
ENST00000257749.9:c.-275+4769G= MANE Select	ENSP00000257749.4:n.-275+4769G=
NM_001170794.1:c.-274-41063G=	NP_001164265.1:n.-274-41063G=
NM_001170794.2:c.-274-41063G=	NP_001164265.1:n.-274-41063G=
NM_021813.3:c.-275+4769G=	NP_068585.1:n.-275+4769G=
ENST00000257749.8:c.-275+4769G=	ENSP00000257749.4:n.-275+4769G=
ENST00000343122.7:c.-269-41068G=	ENSP00000345642.3:n.-269-41068G=
ENST00000406998.6:c.-274-41063G=	ENSP00000384145.2:n.-274-41063G=
ENST00000406998.7:c.-274-41063G=	ENSP00000384145.3:n.-274-41063G=
ENST00000453877.5:c.-270+24105G=	ENSP00000397668.1:n.-270+24105G=
ENST00000453877.6:c.-270+24105G=	ENSP00000397668.2:n.-270+24105G=
ENST00000470301.5:n.356+24105G=
ENST00000470301.6:n.356+24105G=
ENST00000472023.5:n.341+4769G=
ENST00000494747.2:n.356+24105G=
ENST00000537989.5:c.-274-41063G=	ENSP00000437473.1:n.-274-41063G=
ENST00000695953.1:n.361+24105G=
XM_011536037.1:c.-275+24105G=	XP_011534339.1:n.-275+24105G=
XM_011536038.1:c.-354-41063G=	XP_011534340.1:n.-354-41063G=
XM_011536039.1:c.-275+4769G=	XP_011534341.1:n.-275+4769G=
XM_011536039.3:c.-275+4769G=	XP_011534341.1:n.-275+4769G=
XM_011536041.1:c.-269-41068G=	XP_011534343.1:n.-269-41068G=
XM_011536042.1:c.-73-41063G=	XP_011534344.1:n.-73-41063G=
XM_011536043.1:c.-73-41063G=	XP_011534345.1:n.-73-41063G=
XM_017011166.2:c.-355+4769G=	XP_016866655.1:n.-355+4769G=
XM_017011167.2:c.-985+4769G=	XP_016866656.1:n.-985+4769G=
XM_024446513.1:c.-275+24105G=	XP_024302281.1:n.-275+24105G=