Canonical Allele Identifier: CA451581381

Gene: SOBP

Linked Data

• dbSNP Id: rs1770911554
• MyVariant Identifiers: chr6:g.107955857C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634653C>T , CM000668.2:g.107634653C>T	GRCh38
NC_000006.11:g.107955857C>T , CM000668.1:g.107955857C>T	GRCh37
NC_000006.10:g.108062550C>T	NCBI36
NG_028200.1:g.149541C>T
NG_028200.2:g.149541C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1809C>T MANE Select	ENSP00000318900.5:p.Gly603=
ENST00000317357.9:c.1809C>T	ENSP00000318900.5:p.Gly603=
NM_018013.3:c.1809C>T	NP_060483.3:p.Gly603=
XM_005267041.3:c.1962C>T	XP_005267098.1:p.Gly654=
XM_005267042.3:c.1866C>T	XP_005267099.1:p.Gly622=
XM_011535920.1:c.1962C>T	XP_011534222.1:p.Gly654=
XM_011535921.1:c.1848C>T	XP_011534223.1:p.Gly616=
XM_011535922.1:c.1221C>T	XP_011534224.1:p.Gly407=
XM_011535923.1:c.1032C>T	XP_011534225.1:p.Gly344=
XM_005267041.4:c.1962C>T	XP_005267098.1:p.Gly654=
XM_005267042.4:c.1866C>T	XP_005267099.1:p.Gly622=
XM_011535920.2:c.1962C>T	XP_011534222.1:p.Gly654=
XM_011535921.2:c.1848C>T	XP_011534223.1:p.Gly616=
XM_011535923.2:c.1032C>T	XP_011534225.1:p.Gly344=
XM_017010991.1:c.1362C>T	XP_016866480.1:p.Gly454=
XM_017010992.1:c.1362C>T	XP_016866481.1:p.Gly454=
XM_017010993.1:c.1362C>T	XP_016866482.1:p.Gly454=
XM_017010994.1:c.1362C>T	XP_016866483.1:p.Gly454=
NM_018013.4:c.1809C>T MANE Select	NP_060483.3:p.Gly603=