Canonical Allele Identifier: CA448707454
Gene: TUBB2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.3225579T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225345T>G , CM000668.2:g.3225345T>G GRCh38
NC_000006.11:g.3225579T>G , CM000668.1:g.3225579T>G GRCh37
NC_000006.10:g.3170578T>G NCBI36
NG_016715.1:g.7390A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.744A>C MANE Select ENSP00000259818.6:p.Ala248=
ENST00000680070.1:n.1674A>C
ENST00000681707.1:n.1571A>C
ENST00000681757.1:n.1049A>C
ENST00000259818.7:c.744A>C ENSP00000259818.6:p.Ala248=
ENST00000473006.1:n.861A>C
NM_178012.4:c.744A>C NP_821080.1:p.Ala248=
XM_011514571.1:c.528A>C XP_011512873.1:p.Ala176=
NM_178012.5:c.744A>C MANE Select NP_821080.1:p.Ala248=