Canonical Allele Identifier: CA365171774

Gene: SOBP

Linked Data

• dbSNP Id: rs1231573103
• gnomAD v3: 6-107634870-G-A
• gnomAD v4: 6-107634870-G-A
• MyVariant Identifiers: chr6:g.107956074G>A (hg19) ; chr6:g.107634870G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634870G>A , CM000668.2:g.107634870G>A	GRCh38
NC_000006.11:g.107956074G>A , CM000668.1:g.107956074G>A	GRCh37
NC_000006.10:g.108062767G>A	NCBI36
NG_028200.1:g.149758G>A
NG_028200.2:g.149758G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.2026G>A MANE Select	ENSP00000318900.5:p.Val676Ile
ENST00000317357.9:c.2026G>A	ENSP00000318900.5:p.Val676Ile
NM_018013.3:c.2026G>A	NP_060483.3:p.Val676Ile
XM_005267041.3:c.2179G>A	XP_005267098.1:p.Val727Ile
XM_005267042.3:c.2083G>A	XP_005267099.1:p.Val695Ile
XM_011535920.1:c.2179G>A	XP_011534222.1:p.Val727Ile
XM_011535921.1:c.2065G>A	XP_011534223.1:p.Val689Ile
XM_011535922.1:c.1438G>A	XP_011534224.1:p.Val480Ile
XM_011535923.1:c.1249G>A	XP_011534225.1:p.Val417Ile
XM_005267041.4:c.2179G>A	XP_005267098.1:p.Val727Ile
XM_005267042.4:c.2083G>A	XP_005267099.1:p.Val695Ile
XM_011535920.2:c.2179G>A	XP_011534222.1:p.Val727Ile
XM_011535921.2:c.2065G>A	XP_011534223.1:p.Val689Ile
XM_011535923.2:c.1249G>A	XP_011534225.1:p.Val417Ile
XM_017010991.1:c.1579G>A	XP_016866480.1:p.Val527Ile
XM_017010992.1:c.1579G>A	XP_016866481.1:p.Val527Ile
XM_017010993.1:c.1579G>A	XP_016866482.1:p.Val527Ile
XM_017010994.1:c.1579G>A	XP_016866483.1:p.Val527Ile
NM_018013.4:c.2026G>A MANE Select	NP_060483.3:p.Val676Ile