Canonical Allele Identifier: CA1717047178
Gene: BAZ1B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.73442580C= , CM000669.2:g.73442580C= GRCh38
NC_000007.13:g.72856910C= , CM000669.1:g.72856910C= GRCh37
NC_000007.12:g.72494846C= NCBI36
NG_027679.1:g.84706G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000339594.9:c.4095-27G= MANE Select ENSP00000342434.4:n.4095-27G=
ENST00000339594.8:c.4095-27G= ENSP00000342434.4:n.4095-27G=
ENST00000404251.1:c.4095-27G= ENSP00000385442.1:n.4095-27G=
NM_032408.3:c.4095-27G= NP_115784.1:n.4095-27G=
XM_017012773.2:c.4095-27G= XP_016868262.1:n.4095-27G=
NM_032408.4:c.4095-27G= MANE Select NP_115784.1:n.4095-27G=
NM_001370402.1:c.4095-27G= NP_001357331.1:n.4095-27G=
Search 100 bp 5'
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