Canonical Allele Identifier: CA475372169

Gene: SPTBN2

Linked Data

• MyVariant Identifiers: chr11:g.66466164C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66698693C>T , CM000673.2:g.66698693C>T	GRCh38
NC_000011.9:g.66466164C>T , CM000673.1:g.66466164C>T	GRCh37
NC_000011.8:g.66222740C>T	NCBI36
NG_016150.1:g.27707G>A
NG_016150.2:g.35669G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000309996.7:c.3960G>A	ENSP00000311489.2:p.Gln1320=
ENST00000611817.5:c.3960G>A	ENSP00000480692.2:p.Gln1320=
ENST00000617502.5:c.3981G>A	ENSP00000482000.2:p.Gln1327=
ENST00000647510.2:c.3960G>A	ENSP00000508362.1:p.Gln1320=
ENST00000682471.1:n.77G>A
ENST00000533211.6:c.3960G>A MANE Select	ENSP00000432568.1:p.Gln1320=
ENST00000647510.1:n.4487G>A
ENST00000309996.6:c.3960G>A	ENSP00000311489.2:p.Gln1320=
ENST00000529997.5:c.3960G>A	ENSP00000433593.1:p.Gln1320=
ENST00000530665.1:n.115G>A
ENST00000533211.5:c.3960G>A	ENSP00000432568.1:p.Gln1320=
ENST00000611817.4:c.1854+6729G>A	ENSP00000480692.1:n.1854+6729G>A
ENST00000617502.4:c.1845+6738G>A	ENSP00000482000.1:n.1845+6738G>A
NM_006946.2:c.3960G>A	NP_008877.1:p.Gln1320=
XM_005274192.3:c.3960G>A	XP_005274249.1:p.Gln1320=
XM_005274193.3:c.3960G>A	XP_005274250.1:p.Gln1320=
XM_006718669.2:c.3981G>A	XP_006718732.1:p.Gln1327=
XM_006718671.2:c.3960G>A	XP_006718734.1:p.Gln1320=
XM_011545216.1:c.3981G>A	XP_011543518.1:p.Gln1327=
XM_011545217.1:c.3981G>A	XP_011543519.1:p.Gln1327=
NM_006946.3:c.3960G>A	NP_008877.1:p.Gln1320=
XM_005274192.4:c.3960G>A	XP_005274249.1:p.Gln1320=
XM_006718669.3:c.3981G>A	XP_006718732.1:p.Gln1327=
XM_006718671.4:c.3960G>A	XP_006718734.1:p.Gln1320=
XM_011545216.3:c.3981G>A	XP_011543518.1:p.Gln1327=
XM_011545217.2:c.3981G>A	XP_011543519.1:p.Gln1327=
XM_017018174.1:c.3960G>A	XP_016873663.1:p.Gln1320=
XM_017018175.2:c.3960G>A	XP_016873664.1:p.Gln1320=
XM_017018176.1:c.3960G>A	XP_016873665.1:p.Gln1320=
XM_017018177.2:c.3960G>A	XP_016873666.1:p.Gln1320=
XM_017018178.1:c.3960G>A	XP_016873667.1:p.Gln1320=
NM_006946.4:c.3960G>A MANE Select	NP_008877.2:p.Gln1320=