Canonical Allele Identifier: CA367787662
Gene: BAZ1B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.73442527T>A , CM000669.2:g.73442527T>A GRCh38
NC_000007.13:g.72856857T>A , CM000669.1:g.72856857T>A GRCh37
NC_000007.12:g.72494793T>A NCBI36
NG_027679.1:g.84759A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000339594.9:c.4121A>T MANE Select ENSP00000342434.4:p.Glu1374Val
ENST00000339594.8:c.4121A>T ENSP00000342434.4:p.Glu1374Val
ENST00000404251.1:c.4121A>T ENSP00000385442.1:p.Glu1374Val
NM_032408.3:c.4121A>T NP_115784.1:p.Glu1374Val
XM_017012773.2:c.4121A>T XP_016868262.1:p.Glu1374Val
NM_032408.4:c.4121A>T MANE Select NP_115784.1:p.Glu1374Val
NM_001370402.1:c.4121A>T NP_001357331.1:p.Glu1374Val