Canonical Allele Identifier: CA448708269

Gene: TUBB2B

Linked Data

• MyVariant Identifiers: chr6:g.3225999C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.3225765C>T , CM000668.2:g.3225765C>T	GRCh38
NC_000006.11:g.3225999C>T , CM000668.1:g.3225999C>T	GRCh37
NC_000006.10:g.3170998C>T	NCBI36
NG_016715.1:g.6970G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000259818.8:c.324G>A MANE Select	ENSP00000259818.6:p.Glu108=
ENST00000680070.1:n.1254G>A
ENST00000681707.1:n.1151G>A
ENST00000681757.1:n.629G>A
ENST00000259818.7:c.324G>A	ENSP00000259818.6:p.Glu108=
ENST00000473006.1:n.441G>A
NM_178012.4:c.324G>A	NP_821080.1:p.Glu108=
XM_011514571.1:c.108G>A	XP_011512873.1:p.Glu36=
NM_178012.5:c.324G>A MANE Select	NP_821080.1:p.Glu108=