Canonical Allele Identifier: CA363141501

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30688333G>C (hg19) ; chr6:g.30720556G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30720556G>C , CM000668.2:g.30720556G>C	GRCh38
NC_000006.11:g.30688333G>C , CM000668.1:g.30688333G>C	GRCh37
NC_000006.10:g.30796312G>C	NCBI36
NG_034142.1:g.5356G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000327892.13:c.50G>C MANE Select	ENSP00000339001.7:p.Gly17Ala
ENST00000681435.1:c.-159-1981G>C	ENSP00000506665.1:n.-159-1981G>C
ENST00000327892.12:c.50G>C	ENSP00000339001.7:p.Gly17Ala
NM_001293213.1:c.50G>C	NP_001280142.1:p.Gly17Ala
NM_001293214.1:c.34+16G>C	NP_001280143.1:n.34+16G>C
NM_178014.3:c.50G>C	NP_821133.1:p.Gly17Ala
NR_120608.1:n.356G>C
NM_178014.4:c.50G>C MANE Select	NP_821133.1:p.Gly17Ala
NM_001293213.2:c.50G>C	NP_001280142.1:p.Gly17Ala
NM_001293214.2:c.34+16G>C	NP_001280143.1:n.34+16G>C
NR_120608.2:n.205G>C