Canonical Allele Identifier: CA448707379
Gene: TUBB2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.3225546G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225312G>C , CM000668.2:g.3225312G>C GRCh38
NC_000006.11:g.3225546G>C , CM000668.1:g.3225546G>C GRCh37
NC_000006.10:g.3170545G>C NCBI36
NG_016715.1:g.7423C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.777C>G MANE Select ENSP00000259818.6:p.Pro259=
ENST00000680070.1:n.1707C>G
ENST00000681707.1:n.1604C>G
ENST00000681757.1:n.1082C>G
ENST00000259818.7:c.777C>G ENSP00000259818.6:p.Pro259=
ENST00000473006.1:n.894C>G
NM_178012.4:c.777C>G NP_821080.1:p.Pro259=
XM_011514571.1:c.561C>G XP_011512873.1:p.Pro187=
NM_178012.5:c.777C>G MANE Select NP_821080.1:p.Pro259=
Search 100 bp 5'
Search 100 bp 3'