Canonical Allele Identifier: CA1717046908
Gene: BAZ1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.73441946G= , CM000669.2:g.73441946G= GRCh38
NC_000007.13:g.72856276G= , CM000669.1:g.72856276G= GRCh37
NC_000007.12:g.72494212G= NCBI36
NG_027679.1:g.85340C=

Transcript Alleles

HGVS Amino-acid change
ENST00000339594.9:c.*15+235C= MANE Select ENSP00000342434.4:n.*15+235C=
ENST00000339594.8:c.*15+235C= ENSP00000342434.4:n.*15+235C=
ENST00000404251.1:c.*250C= ENSP00000385442.1:n.*250C=
NM_032408.3:c.*15+235C= NP_115784.1:n.*15+235C=
XM_017012773.2:c.*250C= XP_016868262.1:n.*250C=
NM_032408.4:c.*15+235C= MANE Select NP_115784.1:n.*15+235C=
NM_001370402.1:c.*250C= NP_001357331.1:n.*250C=