Canonical Allele Identifier: CA250740
Gene: TUBB2B HGNC NCBI

Linked Data

ClinVar Variation Id: 39721
ClinVar RCV Id: RCV000032933
dbSNP Id: rs397514568
MyVariant Identifiers: chr6:g.3225556T>C (hg19) chr6:g.3225322T>C (hg38)
PubMed: PMID:22333901
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225322T>C , CM000668.2:g.3225322T>C GRCh38
NC_000006.11:g.3225556T>C , CM000668.1:g.3225556T>C GRCh37
NC_000006.10:g.3170555T>C NCBI36
NG_016715.1:g.7413A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000259818.8:c.767A>G MANE Select ENSP00000259818.6:p.Asn256Ser
ENST00000680070.1:n.1697A>G
ENST00000681707.1:n.1594A>G
ENST00000681757.1:n.1072A>G
ENST00000259818.7:c.767A>G ENSP00000259818.6:p.Asn256Ser
ENST00000473006.1:n.884A>G
NM_178012.4:c.767A>G NP_821080.1:p.Asn256Ser
XM_011514571.1:c.551A>G XP_011512873.1:p.Asn184Ser
NM_178012.5:c.767A>G MANE Select NP_821080.1:p.Asn256Ser
Search 100 bp 5'
Search 100 bp 3'