Canonical Allele Identifier: CA251183
Gene: TUBB2B HGNC NCBI

Linked Data

ClinVar Variation Id: 160184
ClinVar RCV Id: RCV000993525 RCV002492538
dbSNP Id: rs587784500
ExAC: 6:3225620 C / T
gnomAD v2: 6-3225620-C-T
gnomAD v3: 6-3225386-C-T
gnomAD v4: 6-3225386-C-T
MyVariant Identifiers: chr6:g.3225620C>T (hg19) chr6:g.3225386C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225386C>T , CM000668.2:g.3225386C>T GRCh38
NC_000006.11:g.3225620C>T , CM000668.1:g.3225620C>T GRCh37
NC_000006.10:g.3170619C>T NCBI36
NG_016715.1:g.7349G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.703G>A MANE Select ENSP00000259818.6:p.Gly235Arg
ENST00000680070.1:n.1633G>A
ENST00000681707.1:n.1530G>A
ENST00000681757.1:n.1008G>A
ENST00000259818.7:c.703G>A ENSP00000259818.6:p.Gly235Arg
ENST00000473006.1:n.820G>A
NM_178012.4:c.703G>A NP_821080.1:p.Gly235Arg
XM_011514571.1:c.487G>A XP_011512873.1:p.Gly163Arg
NM_178012.5:c.703G>A MANE Select NP_821080.1:p.Gly235Arg
Search 100 bp 5'
Search 100 bp 3'