Canonical Allele Identifier: CA3619207
Gene: TUBB2B HGNC NCBI

Linked Data

dbSNP Id: rs760721832
ExAC: 6:3225978 C / G
gnomAD v2: 6-3225978-C-G
gnomAD v4: 6-3225744-C-G
MyVariant Identifiers: chr6:g.3225978C>G (hg19) chr6:g.3225744C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3225744C>G , CM000668.2:g.3225744C>G GRCh38
NC_000006.11:g.3225978C>G , CM000668.1:g.3225978C>G GRCh37
NC_000006.10:g.3170977C>G NCBI36
NG_016715.1:g.6991G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000259818.8:c.345G>C MANE Select ENSP00000259818.6:p.Ser115=
ENST00000680070.1:n.1275G>C
ENST00000681707.1:n.1172G>C
ENST00000681757.1:n.650G>C
ENST00000259818.7:c.345G>C ENSP00000259818.6:p.Ser115=
ENST00000473006.1:n.462G>C
NM_178012.4:c.345G>C NP_821080.1:p.Ser115=
XM_011514571.1:c.129G>C XP_011512873.1:p.Ser43=
NM_178012.5:c.345G>C MANE Select NP_821080.1:p.Ser115=
Search 100 bp 5'
Search 100 bp 3'