Canonical Allele Identifier: CA448708124
Gene: TUBB2B HGNC NCBI

Linked Data

gnomAD v4: 6-3225567-C-T
MyVariant Identifiers: chr6:g.3225801C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225567C>T , CM000668.2:g.3225567C>T GRCh38
NC_000006.11:g.3225801C>T , CM000668.1:g.3225801C>T GRCh37
NC_000006.10:g.3170800C>T NCBI36
NG_016715.1:g.7168G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000259818.8:c.522G>A MANE Select ENSP00000259818.6:p.Lys174=
ENST00000680070.1:n.1452G>A
ENST00000681707.1:n.1349G>A
ENST00000681757.1:n.827G>A
ENST00000259818.7:c.522G>A ENSP00000259818.6:p.Lys174=
ENST00000473006.1:n.639G>A
NM_178012.4:c.522G>A NP_821080.1:p.Lys174=
XM_011514571.1:c.306G>A XP_011512873.1:p.Lys102=
NM_178012.5:c.522G>A MANE Select NP_821080.1:p.Lys174=