Canonical Allele Identifier: CA217415213

Gene: TUB

Linked Data

• dbSNP Id: rs960534110
• MyVariant Identifiers: chr11:g.8111259T>C (hg19) ; chr11:g.8089712T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089712T>C , CM000673.2:g.8089712T>C	GRCh38
NC_000011.9:g.8111259T>C , CM000673.1:g.8111259T>C	GRCh37
NC_000011.8:g.8067835T>C	NCBI36
NG_029912.1:g.56080T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.90+51T>C MANE Select	ENSP00000299506.3:n.90+51T>C
ENST00000299506.2:c.90+51T>C	ENSP00000299506.2:n.90+51T>C
ENST00000305253.8:c.255+51T>C	ENSP00000305426.4:n.255+51T>C
ENST00000534099.5:c.108+51T>C	ENSP00000434400.1:n.108+51T>C
NM_003320.4:c.255+51T>C	NP_003311.2:n.255+51T>C
NM_177972.2:c.90+51T>C	NP_813977.1:n.90+51T>C
XM_005253109.2:c.216+51T>C	XP_005253166.1:n.216+51T>C
XM_011520344.1:c.126+51T>C	XP_011518646.1:n.126+51T>C
XM_005253109.3:c.216+51T>C	XP_005253166.1:n.216+51T>C
XM_011520344.2:c.126+51T>C	XP_011518646.1:n.126+51T>C
NM_177972.3:c.90+51T>C MANE Select	NP_813977.1:n.90+51T>C
NM_003320.5:c.255+51T>C	NP_003311.2:n.255+51T>C