Canonical Allele Identifier: CA451582062

Gene: SOBP

Linked Data

• gnomAD v4: 6-107634905-C-G
• MyVariant Identifiers: chr6:g.107956109C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634905C>G , CM000668.2:g.107634905C>G	GRCh38
NC_000006.11:g.107956109C>G , CM000668.1:g.107956109C>G	GRCh37
NC_000006.10:g.108062802C>G	NCBI36
NG_028200.1:g.149793C>G
NG_028200.2:g.149793C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.2061C>G MANE Select	ENSP00000318900.5:p.Arg687=
ENST00000317357.9:c.2061C>G	ENSP00000318900.5:p.Arg687=
NM_018013.3:c.2061C>G	NP_060483.3:p.Arg687=
XM_005267041.3:c.2214C>G	XP_005267098.1:p.Arg738=
XM_005267042.3:c.2118C>G	XP_005267099.1:p.Arg706=
XM_011535920.1:c.2214C>G	XP_011534222.1:p.Arg738=
XM_011535921.1:c.2100C>G	XP_011534223.1:p.Arg700=
XM_011535922.1:c.1473C>G	XP_011534224.1:p.Arg491=
XM_011535923.1:c.1284C>G	XP_011534225.1:p.Arg428=
XM_005267041.4:c.2214C>G	XP_005267098.1:p.Arg738=
XM_005267042.4:c.2118C>G	XP_005267099.1:p.Arg706=
XM_011535920.2:c.2214C>G	XP_011534222.1:p.Arg738=
XM_011535921.2:c.2100C>G	XP_011534223.1:p.Arg700=
XM_011535923.2:c.1284C>G	XP_011534225.1:p.Arg428=
XM_017010991.1:c.1614C>G	XP_016866480.1:p.Arg538=
XM_017010992.1:c.1614C>G	XP_016866481.1:p.Arg538=
XM_017010993.1:c.1614C>G	XP_016866482.1:p.Arg538=
XM_017010994.1:c.1614C>G	XP_016866483.1:p.Arg538=
NM_018013.4:c.2061C>G MANE Select	NP_060483.3:p.Arg687=