Canonical Allele Identifier: CA15484522
Gene: BACH2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2289577

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.89930772C>T , CM000668.2:g.89930772C>T GRCh38
NC_000006.10:g.90697212C>T NCBI36
NC_000006.11:g.90640491C>T , CM000668.1:g.90640491C>T GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000257749.8:c.*1636G>A ENSP00000257749.4:p.=
ENST00000537989.5:c.*1636G>A ENSP00000437473.1:p.=
NM_001170794.1:c.*1636G>A VV NP_001164265.1:p.=
NM_021813.3:c.*1636G>A VV NP_068585.1:p.=
XM_005248758.3:c.*1636G>A XP_005248815.1:p.=
XM_005248759.3:c.*1636G>A XP_005248816.1:p.=
XM_011536037.1:c.*1636G>A XP_011534339.1:p.=
XM_011536038.1:c.*1636G>A XP_011534340.1:p.=
XM_011536039.1:c.*1636G>A XP_011534341.1:p.=
XM_011536040.1:c.*1636G>A XP_011534342.1:p.=
XM_011536041.1:c.*1636G>A XP_011534343.1:p.=