Canonical Allele Identifier: CA448708129
Gene: TUBB2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.3225807T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225573T>C , CM000668.2:g.3225573T>C GRCh38
NC_000006.11:g.3225807T>C , CM000668.1:g.3225807T>C GRCh37
NC_000006.10:g.3170806T>C NCBI36
NG_016715.1:g.7162A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000259818.8:c.516A>G MANE Select ENSP00000259818.6:p.Ser172=
ENST00000680070.1:n.1446A>G
ENST00000681707.1:n.1343A>G
ENST00000681757.1:n.821A>G
ENST00000259818.7:c.516A>G ENSP00000259818.6:p.Ser172=
ENST00000473006.1:n.633A>G
NM_178012.4:c.516A>G NP_821080.1:p.Ser172=
XM_011514571.1:c.300A>G XP_011512873.1:p.Ser100=
NM_178012.5:c.516A>G MANE Select NP_821080.1:p.Ser172=
Search 100 bp 5'
Search 100 bp 3'