Canonical Allele Identifier: CA362588220
Gene: TUBB2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1676461
ClinVar RCV Id: RCV002221843
dbSNP Id: rs2113819240
MyVariant Identifiers: chr6:g.3225805G>C (hg19) chr6:g.3225571G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225571G>C , CM000668.2:g.3225571G>C GRCh38
NC_000006.11:g.3225805G>C , CM000668.1:g.3225805G>C GRCh37
NC_000006.10:g.3170804G>C NCBI36
NG_016715.1:g.7164C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.518C>G MANE Select ENSP00000259818.6:p.Pro173Arg
ENST00000680070.1:n.1448C>G
ENST00000681707.1:n.1345C>G
ENST00000681757.1:n.823C>G
ENST00000259818.7:c.518C>G ENSP00000259818.6:p.Pro173Arg
ENST00000473006.1:n.635C>G
NM_178012.4:c.518C>G NP_821080.1:p.Pro173Arg
XM_011514571.1:c.302C>G XP_011512873.1:p.Pro101Arg
NM_178012.5:c.518C>G MANE Select NP_821080.1:p.Pro173Arg
Search 100 bp 5'
Search 100 bp 3'