Canonical Allele Identifier: CA365170459

Gene: SOBP

Linked Data

• dbSNP Id: rs1770891653
• MyVariant Identifiers: chr6:g.107955675A>G (hg19) ; chr6:g.107634471A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634471A>G , CM000668.2:g.107634471A>G	GRCh38
NC_000006.11:g.107955675A>G , CM000668.1:g.107955675A>G	GRCh37
NC_000006.10:g.108062368A>G	NCBI36
NG_028200.1:g.149359A>G
NG_028200.2:g.149359A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1627A>G MANE Select	ENSP00000318900.5:p.Ile543Val
ENST00000317357.9:c.1627A>G	ENSP00000318900.5:p.Ile543Val
NM_018013.3:c.1627A>G	NP_060483.3:p.Ile543Val
XM_005267041.3:c.1780A>G	XP_005267098.1:p.Ile594Val
XM_005267042.3:c.1684A>G	XP_005267099.1:p.Ile562Val
XM_011535920.1:c.1780A>G	XP_011534222.1:p.Ile594Val
XM_011535921.1:c.1666A>G	XP_011534223.1:p.Ile556Val
XM_011535922.1:c.1039A>G	XP_011534224.1:p.Ile347Val
XM_011535923.1:c.850A>G	XP_011534225.1:p.Ile284Val
XM_005267041.4:c.1780A>G	XP_005267098.1:p.Ile594Val
XM_005267042.4:c.1684A>G	XP_005267099.1:p.Ile562Val
XM_011535920.2:c.1780A>G	XP_011534222.1:p.Ile594Val
XM_011535921.2:c.1666A>G	XP_011534223.1:p.Ile556Val
XM_011535923.2:c.850A>G	XP_011534225.1:p.Ile284Val
XM_017010991.1:c.1180A>G	XP_016866480.1:p.Ile394Val
XM_017010992.1:c.1180A>G	XP_016866481.1:p.Ile394Val
XM_017010993.1:c.1180A>G	XP_016866482.1:p.Ile394Val
XM_017010994.1:c.1180A>G	XP_016866483.1:p.Ile394Val
NM_018013.4:c.1627A>G MANE Select	NP_060483.3:p.Ile543Val