Canonical Allele Identifier: CA451581980

Gene: SOBP

Linked Data

• dbSNP Id: rs2115146789
• MyVariant Identifiers: chr6:g.107955803G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634599G>T , CM000668.2:g.107634599G>T	GRCh38
NC_000006.11:g.107955803G>T , CM000668.1:g.107955803G>T	GRCh37
NC_000006.10:g.108062496G>T	NCBI36
NG_028200.1:g.149487G>T
NG_028200.2:g.149487G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1755G>T MANE Select	ENSP00000318900.5:p.Arg585=
ENST00000317357.9:c.1755G>T	ENSP00000318900.5:p.Arg585=
NM_018013.3:c.1755G>T	NP_060483.3:p.Arg585=
XM_005267041.3:c.1908G>T	XP_005267098.1:p.Arg636=
XM_005267042.3:c.1812G>T	XP_005267099.1:p.Arg604=
XM_011535920.1:c.1908G>T	XP_011534222.1:p.Arg636=
XM_011535921.1:c.1794G>T	XP_011534223.1:p.Arg598=
XM_011535922.1:c.1167G>T	XP_011534224.1:p.Arg389=
XM_011535923.1:c.978G>T	XP_011534225.1:p.Arg326=
XM_005267041.4:c.1908G>T	XP_005267098.1:p.Arg636=
XM_005267042.4:c.1812G>T	XP_005267099.1:p.Arg604=
XM_011535920.2:c.1908G>T	XP_011534222.1:p.Arg636=
XM_011535921.2:c.1794G>T	XP_011534223.1:p.Arg598=
XM_011535923.2:c.978G>T	XP_011534225.1:p.Arg326=
XM_017010991.1:c.1308G>T	XP_016866480.1:p.Arg436=
XM_017010992.1:c.1308G>T	XP_016866481.1:p.Arg436=
XM_017010993.1:c.1308G>T	XP_016866482.1:p.Arg436=
XM_017010994.1:c.1308G>T	XP_016866483.1:p.Arg436=
NM_018013.4:c.1755G>T MANE Select	NP_060483.3:p.Arg585=