Canonical Allele Identifier: CA1717046858
Gene: BAZ1B HGNC NCBI

Linked Data

dbSNP Id: rs1787629609

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.73441859_73441860dup , CM000669.2:g.73441859_73441860dup GRCh38
NC_000007.13:g.72856189_72856190dup , CM000669.1:g.72856189_72856190dup GRCh37
NC_000007.12:g.72494125_72494126dup NCBI36
NG_027679.1:g.85426_85427dup

Transcript Alleles

HGVS Amino-acid change
ENST00000339594.9:c.*16-167_*16-166dup MANE Select ENSP00000342434.4:n.*16-167_*16-166dup
ENST00000339594.8:c.*16-167_*16-166dup ENSP00000342434.4:n.*16-167_*16-166dup
ENST00000404251.1:c.*336_*337dup ENSP00000385442.1:n.*336_*337dup
NM_032408.3:c.*16-167_*16-166dup NP_115784.1:n.*16-167_*16-166dup
XM_017012773.2:c.*336_*337dup XP_016868262.1:n.*336_*337dup
NM_032408.4:c.*16-167_*16-166dup MANE Select NP_115784.1:n.*16-167_*16-166dup
NM_001370402.1:c.*336_*337dup NP_001357331.1:n.*336_*337dup