Canonical Allele Identifier: CA15096718
Gene: TRABD2B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11211631

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.47918069A>C , CM000663.2:g.47918069A>C GRCh38
NC_000001.10:g.48383741A>C , CM000663.1:g.48383741A>C GRCh37
NC_000001.9:g.48156328A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001194986.1:c.666+75965T>G VV NP_001181915.1:p.=
XM_006710640.2:c.666+75965T>G XP_006710703.1:p.=
XM_011541442.1:c.666+75965T>G XP_011539744.1:p.=
XM_011541443.1:c.666+75965T>G XP_011539745.1:p.=
XM_011541444.1:c.666+75965T>G XP_011539746.1:p.=
XM_011541445.1:c.666+75965T>G XP_011539747.1:p.=
XR_426606.2:n.1246+75965T>G
XR_946653.1:n.1247+75965T>G
XR_946654.1:n.1247+75965T>G
XM_006710640.4:c.666+75965T>G
XM_011541443.3:c.666+75965T>G
XM_011541444.2:c.666+75965T>G
XM_011541445.3:c.666+75965T>G
XM_017001260.2:c.666+75965T>G XP_016856749.1:p.=
XM_017001261.2:c.666+75965T>G XP_016856750.1:p.=
XM_017001262.2:c.666+75965T>G XP_016856751.1:p.=
XM_024446933.1:c.666+75965T>G XP_024302701.1:p.=
XM_024446935.1:c.666+75965T>G XP_024302703.1:p.=
XR_946654.3:n.1244+75965T>G
ENST00000435576.2:n.179+75965T>G
ENST00000606738.2:c.666+75965T>G ENSP00000476820.1:p.=