Canonical Allele Identifier: CA1717047217
Gene: BAZ1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.73442646G= , CM000669.2:g.73442646G= GRCh38
NC_000007.13:g.72856976G= , CM000669.1:g.72856976G= GRCh37
NC_000007.12:g.72494912G= NCBI36
NG_027679.1:g.84640C=

Transcript Alleles

HGVS Amino-acid change
ENST00000339594.9:c.4094+79C= MANE Select ENSP00000342434.4:n.4094+79C=
ENST00000339594.8:c.4094+79C= ENSP00000342434.4:n.4094+79C=
ENST00000404251.1:c.4094+79C= ENSP00000385442.1:n.4094+79C=
NM_032408.3:c.4094+79C= NP_115784.1:n.4094+79C=
XM_017012773.2:c.4094+79C= XP_016868262.1:n.4094+79C=
NM_032408.4:c.4094+79C= MANE Select NP_115784.1:n.4094+79C=
NM_001370402.1:c.4094+79C= NP_001357331.1:n.4094+79C=