Canonical Allele Identifier: CA823918670
Gene: TUBB2B HGNC NCBI

Linked Data

dbSNP Id: rs1217477053
MyVariant Identifiers: chr6:g.3226146C>T (hg19) chr6:g.3225912C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225912C>T , CM000668.2:g.3225912C>T GRCh38
NC_000006.11:g.3226146C>T , CM000668.1:g.3226146C>T GRCh37
NC_000006.10:g.3171145C>T NCBI36
NG_016715.1:g.6823G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.278-101G>A MANE Select ENSP00000259818.6:n.278-101G>A
ENST00000680070.1:n.1208-101G>A
ENST00000681707.1:n.1105-101G>A
ENST00000681757.1:n.583-101G>A
ENST00000259818.7:c.278-101G>A ENSP00000259818.6:n.278-101G>A
ENST00000473006.1:n.395-101G>A
NM_178012.4:c.278-101G>A NP_821080.1:n.278-101G>A
XM_011514571.1:c.62-101G>A XP_011512873.1:n.62-101G>A
NM_178012.5:c.278-101G>A MANE Select NP_821080.1:n.278-101G>A
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