Canonical Allele Identifier: CA448708134
Gene: TUBB2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.3225816G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225582G>A , CM000668.2:g.3225582G>A GRCh38
NC_000006.11:g.3225816G>A , CM000668.1:g.3225816G>A GRCh37
NC_000006.10:g.3170815G>A NCBI36
NG_016715.1:g.7153C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.507C>T MANE Select ENSP00000259818.6:p.Val169=
ENST00000680070.1:n.1437C>T
ENST00000681707.1:n.1334C>T
ENST00000681757.1:n.812C>T
ENST00000259818.7:c.507C>T ENSP00000259818.6:p.Val169=
ENST00000473006.1:n.624C>T
NM_178012.4:c.507C>T NP_821080.1:p.Val169=
XM_011514571.1:c.291C>T XP_011512873.1:p.Val97=
NM_178012.5:c.507C>T MANE Select NP_821080.1:p.Val169=