Canonical Allele Identifier: CA1717046878
Gene: BAZ1B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.73441891C= , CM000669.2:g.73441891C= GRCh38
NC_000007.13:g.72856221C= , CM000669.1:g.72856221C= GRCh37
NC_000007.12:g.72494157C= NCBI36
NG_027679.1:g.85395G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000339594.9:c.*16-198G= MANE Select ENSP00000342434.4:n.*16-198G=
ENST00000339594.8:c.*16-198G= ENSP00000342434.4:n.*16-198G=
ENST00000404251.1:c.*305G= ENSP00000385442.1:n.*305G=
NM_032408.3:c.*16-198G= NP_115784.1:n.*16-198G=
XM_017012773.2:c.*305G= XP_016868262.1:n.*305G=
NM_032408.4:c.*16-198G= MANE Select NP_115784.1:n.*16-198G=
NM_001370402.1:c.*305G= NP_001357331.1:n.*305G=
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