Canonical Allele Identifier: CA362588623

Gene: TUBB2B

Linked Data

• ClinVar Variation Id: 2573750
• ClinVar RCV Id: RCV003318086
• MyVariant Identifiers: chr6:g.3225871A>G (hg19) ; chr6:g.3225637A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.3225637A>G , CM000668.2:g.3225637A>G	GRCh38
NC_000006.11:g.3225871A>G , CM000668.1:g.3225871A>G	GRCh37
NC_000006.10:g.3170870A>G	NCBI36
NG_016715.1:g.7098T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000259818.8:c.452T>C MANE Select	ENSP00000259818.6:p.Leu151Pro
ENST00000680070.1:n.1382T>C
ENST00000681707.1:n.1279T>C
ENST00000681757.1:n.757T>C
ENST00000259818.7:c.452T>C	ENSP00000259818.6:p.Leu151Pro
ENST00000473006.1:n.569T>C
NM_178012.4:c.452T>C	NP_821080.1:p.Leu151Pro
XM_011514571.1:c.236T>C	XP_011512873.1:p.Leu79Pro
NM_178012.5:c.452T>C MANE Select	NP_821080.1:p.Leu151Pro