Canonical Allele Identifier: CA3946581

Gene: SOBP

Linked Data

• dbSNP Id: rs751613728
• ExAC: 6:107955809 C / T
• gnomAD v2: 6-107955809-C-T
• gnomAD v3: 6-107634605-C-T
• gnomAD v4: 6-107634605-C-T
• MyVariant Identifiers: chr6:g.107955809C>T (hg19) ; chr6:g.107634605C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634605C>T , CM000668.2:g.107634605C>T	GRCh38
NC_000006.11:g.107955809C>T , CM000668.1:g.107955809C>T	GRCh37
NC_000006.10:g.108062502C>T	NCBI36
NG_028200.1:g.149493C>T
NG_028200.2:g.149493C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1761C>T MANE Select	ENSP00000318900.5:p.Ser587=
ENST00000317357.9:c.1761C>T	ENSP00000318900.5:p.Ser587=
NM_018013.3:c.1761C>T	NP_060483.3:p.Ser587=
XM_005267041.3:c.1914C>T	XP_005267098.1:p.Ser638=
XM_005267042.3:c.1818C>T	XP_005267099.1:p.Ser606=
XM_011535920.1:c.1914C>T	XP_011534222.1:p.Ser638=
XM_011535921.1:c.1800C>T	XP_011534223.1:p.Ser600=
XM_011535922.1:c.1173C>T	XP_011534224.1:p.Ser391=
XM_011535923.1:c.984C>T	XP_011534225.1:p.Ser328=
XM_005267041.4:c.1914C>T	XP_005267098.1:p.Ser638=
XM_005267042.4:c.1818C>T	XP_005267099.1:p.Ser606=
XM_011535920.2:c.1914C>T	XP_011534222.1:p.Ser638=
XM_011535921.2:c.1800C>T	XP_011534223.1:p.Ser600=
XM_011535923.2:c.984C>T	XP_011534225.1:p.Ser328=
XM_017010991.1:c.1314C>T	XP_016866480.1:p.Ser438=
XM_017010992.1:c.1314C>T	XP_016866481.1:p.Ser438=
XM_017010993.1:c.1314C>T	XP_016866482.1:p.Ser438=
XM_017010994.1:c.1314C>T	XP_016866483.1:p.Ser438=
NM_018013.4:c.1761C>T MANE Select	NP_060483.3:p.Ser587=