Canonical Allele Identifier: CA449776597

Gene: TUBB

Linked Data

• gnomAD v4: 6-30723842-C-T
• MyVariant Identifiers: chr6:g.30691619C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30723842C>T , CM000668.2:g.30723842C>T	GRCh38
NC_000006.11:g.30691619C>T , CM000668.1:g.30691619C>T	GRCh37
NC_000006.10:g.30799598C>T	NCBI36
NG_034142.1:g.8642C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.780C>T MANE Select	ENSP00000339001.7:p.Phe260=
ENST00000680530.1:n.1642C>T
ENST00000681421.1:n.1846C>T
ENST00000681435.1:c.564C>T	ENSP00000506665.1:p.Phe188=
ENST00000327892.12:c.780C>T	ENSP00000339001.7:p.Phe260=
ENST00000330914.7:c.564C>T	ENSP00000365578.2:p.Phe188=
ENST00000396384.1:c.564C>T	ENSP00000379668.1:p.Phe188=
ENST00000396389.5:c.726C>T	ENSP00000379672.1:p.Phe242=
NM_001293212.1:c.840C>T	NP_001280141.1:p.Phe280=
NM_001293213.1:c.370-196C>T	NP_001280142.1:n.370-196C>T
NM_001293214.1:c.648C>T	NP_001280143.1:p.Phe216=
NM_001293215.1:c.564C>T	NP_001280144.1:p.Phe188=
NM_001293216.1:c.564C>T	NP_001280145.1:p.Phe188=
NM_178014.3:c.780C>T	NP_821133.1:p.Phe260=
NR_120608.1:n.584-97C>T
NM_178014.4:c.780C>T MANE Select	NP_821133.1:p.Phe260=
NM_001293212.2:c.840C>T	NP_001280141.1:p.Phe280=
NM_001293213.2:c.370-196C>T	NP_001280142.1:n.370-196C>T
NM_001293214.2:c.648C>T	NP_001280143.1:p.Phe216=
NM_001293215.2:c.564C>T	NP_001280144.1:p.Phe188=
NM_001293216.2:c.564C>T	NP_001280145.1:p.Phe188=
NR_120608.2:n.433-97C>T