Canonical Allele Identifier: CA1717047269
Gene: BAZ1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.73442726T= , CM000669.2:g.73442726T= GRCh38
NC_000007.13:g.72857056T= , CM000669.1:g.72857056T= GRCh37
NC_000007.12:g.72494992T= NCBI36
NG_027679.1:g.84560A=

Transcript Alleles

HGVS Amino-acid change
ENST00000339594.9:c.4093A= MANE Select ENSP00000342434.4:p.Arg1365=
ENST00000339594.8:c.4093A= ENSP00000342434.4:p.Arg1365=
ENST00000404251.1:c.4093A= ENSP00000385442.1:p.Arg1365=
NM_032408.3:c.4093A= NP_115784.1:p.Arg1365=
XM_017012773.2:c.4093A= XP_016868262.1:p.Arg1365=
NM_032408.4:c.4093A= MANE Select NP_115784.1:p.Arg1365=
NM_001370402.1:c.4093A= NP_001357331.1:p.Arg1365=