Canonical Allele Identifier: CA448708319
Gene: TUBB2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.3226035T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225801T>A , CM000668.2:g.3225801T>A GRCh38
NC_000006.11:g.3226035T>A , CM000668.1:g.3226035T>A GRCh37
NC_000006.10:g.3171034T>A NCBI36
NG_016715.1:g.6934A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.288A>T MANE Select ENSP00000259818.6:p.Gly96=
ENST00000680070.1:n.1218A>T
ENST00000681707.1:n.1115A>T
ENST00000681757.1:n.593A>T
ENST00000259818.7:c.288A>T ENSP00000259818.6:p.Gly96=
ENST00000473006.1:n.405A>T
NM_178012.4:c.288A>T NP_821080.1:p.Gly96=
XM_011514571.1:c.72A>T XP_011512873.1:p.Gly24=
NM_178012.5:c.288A>T MANE Select NP_821080.1:p.Gly96=