Canonical Allele Identifier: CA365170546

Gene: SOBP

Linked Data

• dbSNP Id: rs1770892940
• MyVariant Identifiers: chr6:g.107955684G>A (hg19) ; chr6:g.107634480G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634480G>A , CM000668.2:g.107634480G>A	GRCh38
NC_000006.11:g.107955684G>A , CM000668.1:g.107955684G>A	GRCh37
NC_000006.10:g.108062377G>A	NCBI36
NG_028200.1:g.149368G>A
NG_028200.2:g.149368G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1636G>A MANE Select	ENSP00000318900.5:p.Val546Ile
ENST00000317357.9:c.1636G>A	ENSP00000318900.5:p.Val546Ile
NM_018013.3:c.1636G>A	NP_060483.3:p.Val546Ile
XM_005267041.3:c.1789G>A	XP_005267098.1:p.Val597Ile
XM_005267042.3:c.1693G>A	XP_005267099.1:p.Val565Ile
XM_011535920.1:c.1789G>A	XP_011534222.1:p.Val597Ile
XM_011535921.1:c.1675G>A	XP_011534223.1:p.Val559Ile
XM_011535922.1:c.1048G>A	XP_011534224.1:p.Val350Ile
XM_011535923.1:c.859G>A	XP_011534225.1:p.Val287Ile
XM_005267041.4:c.1789G>A	XP_005267098.1:p.Val597Ile
XM_005267042.4:c.1693G>A	XP_005267099.1:p.Val565Ile
XM_011535920.2:c.1789G>A	XP_011534222.1:p.Val597Ile
XM_011535921.2:c.1675G>A	XP_011534223.1:p.Val559Ile
XM_011535923.2:c.859G>A	XP_011534225.1:p.Val287Ile
XM_017010991.1:c.1189G>A	XP_016866480.1:p.Val397Ile
XM_017010992.1:c.1189G>A	XP_016866481.1:p.Val397Ile
XM_017010993.1:c.1189G>A	XP_016866482.1:p.Val397Ile
XM_017010994.1:c.1189G>A	XP_016866483.1:p.Val397Ile
NM_018013.4:c.1636G>A MANE Select	NP_060483.3:p.Val546Ile