Canonical Allele Identifier: CA362588383
Gene: TUBB2B HGNC NCBI

Linked Data

ClinVar Variation Id: 560248
ClinVar RCV Id: RCV000678308
dbSNP Id: rs1561826815
MyVariant Identifiers: chr6:g.3225832A>G (hg19) chr6:g.3225598A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225598A>G , CM000668.2:g.3225598A>G GRCh38
NC_000006.11:g.3225832A>G , CM000668.1:g.3225832A>G GRCh37
NC_000006.10:g.3170831A>G NCBI36
NG_016715.1:g.7137T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.491T>C MANE Select ENSP00000259818.6:p.Met164Thr
ENST00000680070.1:n.1421T>C
ENST00000681707.1:n.1318T>C
ENST00000681757.1:n.796T>C
ENST00000259818.7:c.491T>C ENSP00000259818.6:p.Met164Thr
ENST00000473006.1:n.608T>C
NM_178012.4:c.491T>C NP_821080.1:p.Met164Thr
XM_011514571.1:c.275T>C XP_011512873.1:p.Met92Thr
NM_178012.5:c.491T>C MANE Select NP_821080.1:p.Met164Thr
Search 100 bp 5'
Search 100 bp 3'