Canonical Allele Identifier: CA6128006

Gene: SPTBN2

Linked Data

• ClinVar Variation Id: 305538
• ClinVar RCV Id: RCV000306514 ; RCV000523983 ; RCV000660459
• dbSNP Id: rs764407421
• ExAC: 11:66455772 C / T
• gnomAD v2: 11-66455772-C-T
• gnomAD v3: 11-66688301-C-T
• gnomAD v4: 11-66688301-C-T
• MyVariant Identifiers: chr11:g.66455772C>T (hg19) ; chr11:g.66688301C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66688301C>T , CM000673.2:g.66688301C>T	GRCh38
NC_000011.9:g.66455772C>T , CM000673.1:g.66455772C>T	GRCh37
NC_000011.8:g.66212348C>T	NCBI36
NG_016150.1:g.38099G>A
NG_016150.2:g.46061G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000309996.7:c.6242G>A	ENSP00000311489.2:p.Arg2081Gln
ENST00000611817.5:c.6242G>A	ENSP00000480692.2:p.Arg2081Gln
ENST00000617502.5:c.6263G>A	ENSP00000482000.2:p.Arg2088Gln
ENST00000647510.2:c.6242G>A	ENSP00000508362.1:p.Arg2081Gln
ENST00000533211.6:c.6242G>A MANE Select	ENSP00000432568.1:p.Arg2081Gln
ENST00000647510.1:n.6769G>A
ENST00000309996.6:c.6242G>A	ENSP00000311489.2:p.Arg2081Gln
ENST00000529997.5:c.6242G>A	ENSP00000433593.1:p.Arg2081Gln
ENST00000532650.1:n.276G>A
ENST00000533211.5:c.6242G>A	ENSP00000432568.1:p.Arg2081Gln
ENST00000611817.4:c.1874G>A	ENSP00000480692.1:p.Arg625Gln
ENST00000617502.4:c.1874G>A	ENSP00000482000.1:p.Arg625Gln
NM_006946.2:c.6242G>A	NP_008877.1:p.Arg2081Gln
XM_005274192.3:c.6242G>A	XP_005274249.1:p.Arg2081Gln
XM_005274193.3:c.6242G>A	XP_005274250.1:p.Arg2081Gln
XM_006718669.2:c.6263G>A	XP_006718732.1:p.Arg2088Gln
XM_006718671.2:c.6242G>A	XP_006718734.1:p.Arg2081Gln
NM_006946.3:c.6242G>A	NP_008877.1:p.Arg2081Gln
XM_005274192.4:c.6242G>A	XP_005274249.1:p.Arg2081Gln
XM_006718669.3:c.6263G>A	XP_006718732.1:p.Arg2088Gln
XM_006718671.4:c.6242G>A	XP_006718734.1:p.Arg2081Gln
XM_017018174.1:c.6242G>A	XP_016873663.1:p.Arg2081Gln
XM_017018175.2:c.6242G>A	XP_016873664.1:p.Arg2081Gln
XM_017018176.1:c.6242G>A	XP_016873665.1:p.Arg2081Gln
XM_017018177.2:c.6242G>A	XP_016873666.1:p.Arg2081Gln
XM_017018178.1:c.6242G>A	XP_016873667.1:p.Arg2081Gln
NM_006946.4:c.6242G>A MANE Select	NP_008877.2:p.Arg2081Gln