Canonical Allele Identifier: CA448707734
Gene: TUBB2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.3225744C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225510C>G , CM000668.2:g.3225510C>G GRCh38
NC_000006.11:g.3225744C>G , CM000668.1:g.3225744C>G GRCh37
NC_000006.10:g.3170743C>G NCBI36
NG_016715.1:g.7225G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.579G>C MANE Select ENSP00000259818.6:p.Val193=
ENST00000680070.1:n.1509G>C
ENST00000681707.1:n.1406G>C
ENST00000681757.1:n.884G>C
ENST00000259818.7:c.579G>C ENSP00000259818.6:p.Val193=
ENST00000473006.1:n.696G>C
NM_178012.4:c.579G>C NP_821080.1:p.Val193=
XM_011514571.1:c.363G>C XP_011512873.1:p.Val121=
NM_178012.5:c.579G>C MANE Select NP_821080.1:p.Val193=
Search 100 bp 5'
Search 100 bp 3'