Canonical Allele Identifier: CA448708107
Gene: TUBB2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.3226044G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225810G>C , CM000668.2:g.3225810G>C GRCh38
NC_000006.11:g.3226044G>C , CM000668.1:g.3226044G>C GRCh37
NC_000006.10:g.3171043G>C NCBI36
NG_016715.1:g.6925C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.279C>G MANE Select ENSP00000259818.6:p.Gly93=
ENST00000680070.1:n.1209C>G
ENST00000681707.1:n.1106C>G
ENST00000681757.1:n.584C>G
ENST00000259818.7:c.279C>G ENSP00000259818.6:p.Gly93=
ENST00000473006.1:n.396C>G
NM_178012.4:c.279C>G NP_821080.1:p.Gly93=
XM_011514571.1:c.63C>G XP_011512873.1:p.Gly21=
NM_178012.5:c.279C>G MANE Select NP_821080.1:p.Gly93=