Canonical Allele Identifier: CA448708109
Gene: TUBB2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.3225783C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225549C>A , CM000668.2:g.3225549C>A GRCh38
NC_000006.11:g.3225783C>A , CM000668.1:g.3225783C>A GRCh37
NC_000006.10:g.3170782C>A NCBI36
NG_016715.1:g.7186G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.540G>T MANE Select ENSP00000259818.6:p.Val180=
ENST00000680070.1:n.1470G>T
ENST00000681707.1:n.1367G>T
ENST00000681757.1:n.845G>T
ENST00000259818.7:c.540G>T ENSP00000259818.6:p.Val180=
ENST00000473006.1:n.657G>T
NM_178012.4:c.540G>T NP_821080.1:p.Val180=
XM_011514571.1:c.324G>T XP_011512873.1:p.Val108=
NM_178012.5:c.540G>T MANE Select NP_821080.1:p.Val180=