Canonical Allele Identifier: CA448708122
Gene: TUBB2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.3225798C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225564C>G , CM000668.2:g.3225564C>G GRCh38
NC_000006.11:g.3225798C>G , CM000668.1:g.3225798C>G GRCh37
NC_000006.10:g.3170797C>G NCBI36
NG_016715.1:g.7171G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000259818.8:c.525G>C MANE Select ENSP00000259818.6:p.Val175=
ENST00000680070.1:n.1455G>C
ENST00000681707.1:n.1352G>C
ENST00000681757.1:n.830G>C
ENST00000259818.7:c.525G>C ENSP00000259818.6:p.Val175=
ENST00000473006.1:n.642G>C
NM_178012.4:c.525G>C NP_821080.1:p.Val175=
XM_011514571.1:c.309G>C XP_011512873.1:p.Val103=
NM_178012.5:c.525G>C MANE Select NP_821080.1:p.Val175=