Canonical Allele Identifier: CA448708235
Gene: TUBB2B HGNC NCBI

Linked Data

dbSNP Id: rs1757279243
MyVariant Identifiers: chr6:g.3225972C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225738C>T , CM000668.2:g.3225738C>T GRCh38
NC_000006.11:g.3225972C>T , CM000668.1:g.3225972C>T GRCh37
NC_000006.10:g.3170971C>T NCBI36
NG_016715.1:g.6997G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.351G>A MANE Select ENSP00000259818.6:p.Leu117=
ENST00000680070.1:n.1281G>A
ENST00000681707.1:n.1178G>A
ENST00000681757.1:n.656G>A
ENST00000259818.7:c.351G>A ENSP00000259818.6:p.Leu117=
ENST00000473006.1:n.468G>A
NM_178012.4:c.351G>A NP_821080.1:p.Leu117=
XM_011514571.1:c.135G>A XP_011512873.1:p.Leu45=
NM_178012.5:c.351G>A MANE Select NP_821080.1:p.Leu117=
Search 100 bp 5'
Search 100 bp 3'