Canonical Allele Identifier: CA448707490
Gene: TUBB2B HGNC NCBI

Linked Data

dbSNP Id: rs1337488114
MyVariant Identifiers: chr6:g.3225600G>A (hg19) chr6:g.3225366G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225366G>A , CM000668.2:g.3225366G>A GRCh38
NC_000006.11:g.3225600G>A , CM000668.1:g.3225600G>A GRCh37
NC_000006.10:g.3170599G>A NCBI36
NG_016715.1:g.7369C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.723C>T MANE Select ENSP00000259818.6:p.Arg241=
ENST00000680070.1:n.1653C>T
ENST00000681707.1:n.1550C>T
ENST00000681757.1:n.1028C>T
ENST00000259818.7:c.723C>T ENSP00000259818.6:p.Arg241=
ENST00000473006.1:n.840C>T
NM_178012.4:c.723C>T NP_821080.1:p.Arg241=
XM_011514571.1:c.507C>T XP_011512873.1:p.Arg169=
NM_178012.5:c.723C>T MANE Select NP_821080.1:p.Arg241=
Search 100 bp 5'
Search 100 bp 3'