Canonical Allele Identifier: CA448707725
Gene: TUBB2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.3225732A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225498A>G , CM000668.2:g.3225498A>G GRCh38
NC_000006.11:g.3225732A>G , CM000668.1:g.3225732A>G GRCh37
NC_000006.10:g.3170731A>G NCBI36
NG_016715.1:g.7237T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.591T>C MANE Select ENSP00000259818.6:p.Asp197=
ENST00000680070.1:n.1521T>C
ENST00000681707.1:n.1418T>C
ENST00000681757.1:n.896T>C
ENST00000259818.7:c.591T>C ENSP00000259818.6:p.Asp197=
ENST00000473006.1:n.708T>C
NM_178012.4:c.591T>C NP_821080.1:p.Asp197=
XM_011514571.1:c.375T>C XP_011512873.1:p.Asp125=
NM_178012.5:c.591T>C MANE Select NP_821080.1:p.Asp197=
Search 100 bp 5'
Search 100 bp 3'