Canonical Allele Identifier: CA362587735

Gene: TUBB2B

Linked Data

• ClinVar Variation Id: 2438435
• ClinVar RCV Id: RCV003139187
• MyVariant Identifiers: chr6:g.3225716C>G (hg19) ; chr6:g.3225482C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.3225482C>G , CM000668.2:g.3225482C>G	GRCh38
NC_000006.11:g.3225716C>G , CM000668.1:g.3225716C>G	GRCh37
NC_000006.10:g.3170715C>G	NCBI36
NG_016715.1:g.7253G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000259818.8:c.607G>C MANE Select	ENSP00000259818.6:p.Asp203His
ENST00000680070.1:n.1537G>C
ENST00000681707.1:n.1434G>C
ENST00000681757.1:n.912G>C
ENST00000259818.7:c.607G>C	ENSP00000259818.6:p.Asp203His
ENST00000473006.1:n.724G>C
NM_178012.4:c.607G>C	NP_821080.1:p.Asp203His
XM_011514571.1:c.391G>C	XP_011512873.1:p.Asp131His
NM_178012.5:c.607G>C MANE Select	NP_821080.1:p.Asp203His