Canonical Allele Identifier: CA448707383
Gene: TUBB2B HGNC NCBI

Linked Data

dbSNP Id: rs1757274512
MyVariant Identifiers: chr6:g.3225549C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225315C>A , CM000668.2:g.3225315C>A GRCh38
NC_000006.11:g.3225549C>A , CM000668.1:g.3225549C>A GRCh37
NC_000006.10:g.3170548C>A NCBI36
NG_016715.1:g.7420G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.774G>T MANE Select ENSP00000259818.6:p.Val258=
ENST00000680070.1:n.1704G>T
ENST00000681707.1:n.1601G>T
ENST00000681757.1:n.1079G>T
ENST00000259818.7:c.774G>T ENSP00000259818.6:p.Val258=
ENST00000473006.1:n.891G>T
NM_178012.4:c.774G>T NP_821080.1:p.Val258=
XM_011514571.1:c.558G>T XP_011512873.1:p.Val186=
NM_178012.5:c.774G>T MANE Select NP_821080.1:p.Val258=
Search 100 bp 5'
Search 100 bp 3'