Canonical Allele Identifier: CA448708118
Gene: TUBB2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.3225795T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225561T>A , CM000668.2:g.3225561T>A GRCh38
NC_000006.11:g.3225795T>A , CM000668.1:g.3225795T>A GRCh37
NC_000006.10:g.3170794T>A NCBI36
NG_016715.1:g.7174A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000259818.8:c.528A>T MANE Select ENSP00000259818.6:p.Ser176=
ENST00000680070.1:n.1458A>T
ENST00000681707.1:n.1355A>T
ENST00000681757.1:n.833A>T
ENST00000259818.7:c.528A>T ENSP00000259818.6:p.Ser176=
ENST00000473006.1:n.645A>T
NM_178012.4:c.528A>T NP_821080.1:p.Ser176=
XM_011514571.1:c.312A>T XP_011512873.1:p.Ser104=
NM_178012.5:c.528A>T MANE Select NP_821080.1:p.Ser176=