Canonical Allele Identifier: CA1717046857
Gene: BAZ1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.73441858T= , CM000669.2:g.73441858T= GRCh38
NC_000007.13:g.72856188T= , CM000669.1:g.72856188T= GRCh37
NC_000007.12:g.72494124T= NCBI36
NG_027679.1:g.85428A=

Transcript Alleles

HGVS Amino-acid change
ENST00000339594.9:c.*16-165A= MANE Select ENSP00000342434.4:n.*16-165A=
ENST00000339594.8:c.*16-165A= ENSP00000342434.4:n.*16-165A=
ENST00000404251.1:c.*338A= ENSP00000385442.1:n.*338A=
NM_032408.3:c.*16-165A= NP_115784.1:n.*16-165A=
XM_017012773.2:c.*338A= XP_016868262.1:n.*338A=
NM_032408.4:c.*16-165A= MANE Select NP_115784.1:n.*16-165A=
NM_001370402.1:c.*338A= NP_001357331.1:n.*338A=