Canonical Allele Identifier: CA1301807832
Gene: BAZ2B HGNC NCBI

Linked Data

dbSNP Id: rs2062401202

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.159318987dup , CM000664.2:g.159318987dup GRCh38
NC_000002.11:g.160175498dup , CM000664.1:g.160175498dup GRCh37
NC_000002.10:g.159883744dup NCBI36
NG_051314.1:g.398453dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000392783.7:c.*1278dup MANE Select ENSP00000376534.2:n.*1278dup
ENST00000392782.5:c.*1278dup ENSP00000376533.1:n.*1278dup
ENST00000392783.6:c.*1278dup ENSP00000376534.2:n.*1278dup
NM_001289975.1:c.*1278dup NP_001276904.1:n.*1278dup
NM_013450.3:c.*1278dup NP_038478.2:n.*1278dup
XM_005246488.2:c.6636+1287dup XP_005246545.2:n.6636+1287dup
XM_005246489.3:c.6636+1287dup XP_005246546.2:n.6636+1287dup
XM_005246492.3:c.6630+1287dup XP_005246549.2:n.6630+1287dup
XM_006712461.2:c.6636+1287dup XP_006712524.2:n.6636+1287dup
XM_011511036.1:c.6687+1287dup XP_011509338.1:n.6687+1287dup
XM_011511037.1:c.6687+1287dup XP_011509339.1:n.6687+1287dup
XM_011511038.1:c.6630+1287dup XP_011509340.1:n.6630+1287dup
XM_011511039.1:c.6603+1287dup XP_011509341.1:n.6603+1287dup
XM_011511040.1:c.6636+1287dup XP_011509342.1:n.6636+1287dup
XM_011511041.1:c.6534+1287dup XP_011509343.1:n.6534+1287dup
XM_011511042.1:c.6531+1287dup XP_011509344.1:n.6531+1287dup
XM_011511043.1:c.6501+1287dup XP_011509345.1:n.6501+1287dup
XM_011511044.1:c.*1278dup XP_011509346.1:n.*1278dup
XM_011511045.1:c.6441+1287dup XP_011509347.1:n.6441+1287dup
XM_011511046.1:c.*1278dup XP_011509348.1:n.*1278dup
XM_011511047.1:c.6447+1287dup XP_011509349.1:n.6447+1287dup
XM_011511048.1:c.6447+1287dup XP_011509350.1:n.6447+1287dup
XM_011511049.1:c.6342+1287dup XP_011509351.1:n.6342+1287dup
XM_011511050.1:c.6336+1287dup XP_011509352.1:n.6336+1287dup
XM_011511051.1:c.*1278dup XP_011509353.1:n.*1278dup
XM_011511052.1:c.6240+1287dup XP_011509354.1:n.6240+1287dup
XM_011511056.1:c.4188+1287dup XP_011509358.1:n.4188+1287dup
XM_011511057.1:c.3630+1287dup XP_011509359.1:n.3630+1287dup
NM_001329857.1:c.*1278dup NP_001316786.1:n.*1278dup
NM_001329858.1:c.*1278dup NP_001316787.1:n.*1278dup
XM_005246489.4:c.6636+1287dup XP_005246546.2:n.6636+1287dup
XM_005246492.4:c.6630+1287dup XP_005246549.2:n.6630+1287dup
XM_011511038.2:c.6630+1287dup XP_011509340.1:n.6630+1287dup
XM_011511048.2:c.6447+1287dup XP_011509350.1:n.6447+1287dup
XM_017003920.1:c.6636+1287dup XP_016859409.1:n.6636+1287dup
XM_017003921.1:c.6630+1287dup XP_016859410.1:n.6630+1287dup
XM_017003922.1:c.6630+1287dup XP_016859411.1:n.6630+1287dup
XM_017003923.1:c.*1278dup XP_016859412.1:n.*1278dup
XM_017003924.1:c.6528+1287dup XP_016859413.1:n.6528+1287dup
XM_017003925.1:c.6534+1287dup XP_016859414.1:n.6534+1287dup
XM_017003926.1:c.6435+1287dup XP_016859415.1:n.6435+1287dup
XM_017003928.1:c.6342+1287dup XP_016859417.1:n.6342+1287dup
XM_017003930.1:c.6336+1287dup XP_016859419.1:n.6336+1287dup
XM_017003931.1:c.6330+1287dup XP_016859420.1:n.6330+1287dup
XM_017003933.1:c.6153+1287dup XP_016859422.1:n.6153+1287dup
XM_017003934.1:c.6147+1287dup XP_016859423.1:n.6147+1287dup
XM_017003935.1:c.6051+1287dup XP_016859424.1:n.6051+1287dup
XM_017003936.1:c.*1278dup XP_016859425.1:n.*1278dup
XM_017003937.1:c.3861+1287dup XP_016859426.1:n.3861+1287dup
XM_024452825.1:c.6687+1287dup XP_024308593.1:n.6687+1287dup
XM_024452826.1:c.6687+1287dup XP_024308594.1:n.6687+1287dup
XM_024452827.1:c.6687+1287dup XP_024308595.1:n.6687+1287dup
XM_024452828.1:c.6636+1287dup XP_024308596.1:n.6636+1287dup
XM_024452829.1:c.6534+1287dup XP_024308597.1:n.6534+1287dup
XR_001738732.1:n.7684dup
XR_001738733.1:n.6397+1287dup
NM_013450.4:c.*1278dup MANE Select NP_038478.2:n.*1278dup
NM_001329857.2:c.*1278dup NP_001316786.1:n.*1278dup
NM_001329858.2:c.*1278dup NP_001316787.1:n.*1278dup