Canonical Allele Identifier: CA15470800
Gene: BACH2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs12204127

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.89988555C>T , CM000668.2:g.89988555C>T GRCh38
NC_000006.11:g.90698274C>T , CM000668.1:g.90698274C>T GRCh37
NC_000006.10:g.90754995C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001170794.1:c.243+20047G>A VV NP_001164265.1:p.=
NM_021813.3:c.243+20047G>A VV NP_068585.1:p.=
XM_005248758.3:c.351+20047G>A XP_005248815.1:p.=
XM_005248759.3:c.243+20047G>A XP_005248816.1:p.=
XM_011536037.1:c.243+20047G>A XP_011534339.1:p.=
XM_011536038.1:c.243+20047G>A XP_011534340.1:p.=
XM_011536039.1:c.243+20047G>A XP_011534341.1:p.=
XM_011536040.1:c.243+20047G>A XP_011534342.1:p.=
XM_011536041.1:c.243+20047G>A XP_011534343.1:p.=
XM_011536042.1:c.549+20047G>A XP_011534344.1:p.=
XM_011536043.1:c.549+20047G>A XP_011534345.1:p.=
XM_005248758.5:c.351+20047G>A XP_005248815.1:p.=
XM_005248759.5:c.243+20047G>A XP_005248816.1:p.=
XM_011536039.3:c.243+20047G>A XP_011534341.1:p.=
XM_011536040.2:c.243+20047G>A XP_011534342.1:p.=
XM_017011166.2:c.243+20047G>A XP_016866655.1:p.=
XM_017011167.2:c.501+20047G>A XP_016866656.1:p.=
XM_024446510.1:c.501+20047G>A XP_024302278.1:p.=
XM_024446511.1:c.501+20047G>A XP_024302279.1:p.=
XM_024446513.1:c.243+20047G>A XP_024302281.1:p.=
NM_021813.4:c.243+20047G>A VV MANE Preferred NP_068585.1:p.=
ENST00000257749.8:c.243+20047G>A ENSP00000257749.4:p.=
ENST00000343122.7:c.243+20047G>A ENSP00000345642.3:p.=
ENST00000537989.5:c.243+20047G>A ENSP00000437473.1:p.=