Canonical Allele Identifier: CA448707589
Gene: TUBB2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.3225648G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225414G>C , CM000668.2:g.3225414G>C GRCh38
NC_000006.11:g.3225648G>C , CM000668.1:g.3225648G>C GRCh37
NC_000006.10:g.3170647G>C NCBI36
NG_016715.1:g.7321C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.675C>G MANE Select ENSP00000259818.6:p.Leu225=
ENST00000680070.1:n.1605C>G
ENST00000681707.1:n.1502C>G
ENST00000681757.1:n.980C>G
ENST00000259818.7:c.675C>G ENSP00000259818.6:p.Leu225=
ENST00000473006.1:n.792C>G
NM_178012.4:c.675C>G NP_821080.1:p.Leu225=
XM_011514571.1:c.459C>G XP_011512873.1:p.Leu153=
NM_178012.5:c.675C>G MANE Select NP_821080.1:p.Leu225=