Canonical Allele Identifier: CA448707386
Gene: TUBB2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.3225549C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225315C>G , CM000668.2:g.3225315C>G GRCh38
NC_000006.11:g.3225549C>G , CM000668.1:g.3225549C>G GRCh37
NC_000006.10:g.3170548C>G NCBI36
NG_016715.1:g.7420G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.774G>C MANE Select ENSP00000259818.6:p.Val258=
ENST00000680070.1:n.1704G>C
ENST00000681707.1:n.1601G>C
ENST00000681757.1:n.1079G>C
ENST00000259818.7:c.774G>C ENSP00000259818.6:p.Val258=
ENST00000473006.1:n.891G>C
NM_178012.4:c.774G>C NP_821080.1:p.Val258=
XM_011514571.1:c.558G>C XP_011512873.1:p.Val186=
NM_178012.5:c.774G>C MANE Select NP_821080.1:p.Val258=